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dbVar

Database of genomic structural variation

nsv5536419

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:38

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: 125 SVs from 21 studies. See in: genome view

Submitted genomic33,831,745-33,831,782

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5536419	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000020.11	Chr20	33,831,745	33,831,782
nsv5536419	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000020.10	Chr20	32,419,551	32,419,588

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17732051	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17732051	Submitted genomic		NC_000020.11:g.338 31745_33831782ins1 62	GRCh38 (hg38)		NC_000020.11	Chr20	33,831,745	33,831,782
nssv17732051	Remapped	Perfect	NC_000020.10:g.324 19551_32419588ins1 62	GRCh37.p13	First Pass	NC_000020.10	Chr20	32,419,551	32,419,588

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)
nssv17732051	0.001	7	6404

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