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dbVar

Database of genomic structural variation

nsv4337628

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:9,100,729

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: 6270 SVs from 23 studies. See in: genome view

Remapped(Score: Perfect):95,051,433-104,152,161

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4337628	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	95,051,433	104,152,161
nsv4337628	Submitted genomic		GRCh37.p13	Primary Assembly		NC_000004.11	Chr4	95,972,584	105,073,318

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15790270	sequence alteration	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15790270	Remapped	Perfect	GRCh38.p12	First Pass	NC_000004.12	Chr4	95,051,433	104,152,161
nssv15790270	Submitted genomic		GRCh37.p13		NC_000004.11	Chr4	95,972,584	105,073,318

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)
nssv15790270	4.6e-005	1	21694

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