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dbVar

Database of genomic structural variation

nsv5913135

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:144

Publication(s):Almarri et al. 2020

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: 310 SVs from 52 studies. See in: genome view

Submitted genomic151,360,895-151,361,038

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5913135	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	151,360,895	151,361,038
nsv5913135	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	151,057,981	151,058,124

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17437278	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17437278	Submitted genomic		NC_000007.14:g.151 360895_151361038de l	GRCh38 (hg38)		NC_000007.14	Chr7	151,360,895	151,361,038
nssv17437278	Remapped	Perfect	NC_000007.13:g.151 057981_151058124de l	GRCh37.p13	First Pass	NC_000007.13	Chr7	151,057,981	151,058,124

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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