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dbVar

Database of genomic structural variation

nsv5516108

Organism: Homo sapiens

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

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:779

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: 92 SVs from 24 studies. See in: genome view

Submitted genomic10,281,260-10,282,038

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5516108	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	10,281,260	10,282,038
nsv5516108	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	10,391,936	10,392,714

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17721299	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17721299	Submitted genomic		NC_000019.10:g.102 81260_10282038del	GRCh38 (hg38)		NC_000019.10	Chr19	10,281,260	10,282,038
nssv17721299	Remapped	Perfect	NC_000019.9:g.1039 1936_10392714del	GRCh37.p13	First Pass	NC_000019.9	Chr19	10,391,936	10,392,714

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)
nssv17721299	<0.001	1	6404

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