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dbVar

Database of genomic structural variation

nsv4319221

Organism: Homo sapiens

Study:nstd166 (gnomAD Structural Variants)
Variant Type:sequence alteration
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1,600

Description:complex variant
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: 96 SVs from 6 studies. See in: genome view

Remapped(Score: Perfect):20,754,592-20,756,191

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4319221	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000024.10	ChrY	20,754,592	20,756,191
nsv4319221	Submitted genomic		GRCh37.p13	Primary Assembly		NC_000024.9	ChrY	22,916,478	22,918,077

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15791835	sequence alteration	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15791835	Remapped	Perfect	GRCh38.p12	First Pass	NC_000024.10	ChrY	20,754,592	20,756,191
nssv15791835	Submitted genomic		GRCh37.p13		NC_000024.9	ChrY	22,916,478	22,918,077

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)
nssv15791835	<0.001	2	11056

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