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dbVar

Database of genomic structural variation

nsv4766337

Organism: Homo sapiens

Study:nstd199 (Quan et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh37

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

Publication(s):Quan et al. 2021

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: 388 SVs from 34 studies. See in: genome view

Remapped(Score: Perfect):1,429,100-1,429,100

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4766337	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	1,429,100	1,429,100
nsv4766337	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	1,479,101	1,479,101

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16267539	insertion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16267539	Remapped	Perfect	NC_000016.10:g.142 9100_1429101ins52	GRCh38.p12	First Pass	NC_000016.10	Chr16	1,429,100	1,429,100
nssv16267539	Submitted genomic		NC_000016.9:g.1479 101_1479102ins52	GRCh37 (hg19)		NC_000016.9	Chr16	1,479,101	1,479,101

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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