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dbVar

Database of genomic structural variation

nsv499815

Organism: Homo sapiens

Study:nstd47 (Kidd et al. 2010b)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:NCBI36 (hg18)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:4,266

Publication(s):Kidd et al. 2010

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 353 SVs from 48 studies. See in: genome view

Remapped(Score: Perfect):234,645,379-234,649,644

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv499815	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	234,645,379	234,649,644
nsv499815	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	235,554,023	235,558,288
nsv499815	Submitted genomic		NCBI36 (hg18)	Primary Assembly		NC_000002.10	Chr2	235,218,762	235,223,027

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv585636	copy number loss	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv585636	Remapped	Perfect	NC_000002.12:g.234 645379_234649644de l	GRCh38.p12	First Pass	NC_000002.12	Chr2	234,645,379	234,649,644
nssv585636	Remapped	Perfect	NC_000002.11:g.235 554023_235558288de l	GRCh37.p13	First Pass	NC_000002.11	Chr2	235,554,023	235,558,288
nssv585636	Submitted genomic		NC_000002.10:g.235 218762_235223027de l	NCBI36 (hg18)		NC_000002.10	Chr2	235,218,762	235,223,027

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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