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dbVar

Database of genomic structural variation

nsv4341038

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:2

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: 38 SVs from 5 studies. See in: genome view

Remapped(Score: Perfect):58,432,879-58,432,880

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4341038	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	58,432,879	58,432,880
nsv4341038	Submitted genomic		GRCh37.p13	Primary Assembly		NC_000008.10	Chr8	59,345,438	59,345,439

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15791377	sequence alteration	Sequencing	Other

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv15791377	Remapped	Perfect	GRCh38.p12	First Pass	NC_000008.11	Chr8	58,432,879	58,432,880
nssv15791377	Submitted genomic		GRCh37.p13		NC_000008.10	Chr8	59,345,438	59,345,439

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)
nssv15791377	4.6e-005	1	21694

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