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dbVar

Database of genomic structural variation

nsv5561330

Organism: Homo sapiens

Study:nstd206 (Byrska-Bishop et al. 2022)
Variant Type:sequence alteration
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:4,726,391

Description:complex variant
Publication(s):Byrska-Bishop et al. 2022

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: 12372 SVs from 108 studies. See in: genome view

Submitted genomic44,983,377-49,709,767

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5561330	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000013.11	Chr13	44,983,377	49,709,767
nsv5561330	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000013.10	Chr13	45,557,512	50,283,903

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17687373	sequence alteration	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17687373	Submitted genomic		GRCh38 (hg38)		NC_000013.11	Chr13	44,983,377	49,709,767
nssv17687373	Remapped	Perfect	GRCh37.p13	First Pass	NC_000013.10	Chr13	45,557,512	50,283,903

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)
nssv17687373	<0.001	1	6404

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