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dbVar

Database of genomic structural variation

nsv4139896

Organism: Homo sapiens

Study:nstd166 (gnomAD Structural Variants)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1,772

Publication(s):gnomAD_Structural_Variants

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: 37 SVs from 7 studies. See in: genome view

Remapped(Score: Perfect):35,768,428-35,770,199

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4139896	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	35,768,428	35,770,199
nsv4139896	Submitted genomic		GRCh37.p13	Primary Assembly		NC_000007.13	Chr7	35,808,038	35,809,809

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15920232	deletion	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15920232	Remapped	Perfect	NC_000007.14:g.357 68428_35770199del	GRCh38.p12	First Pass	NC_000007.14	Chr7	35,768,428	35,770,199
nssv15920232	Submitted genomic		NC_000007.13:g.358 08038_35809809del	GRCh37.p13		NC_000007.13	Chr7	35,808,038	35,809,809

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv15920232	<0.001	4	21694

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