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dbVar

Database of genomic structural variation

nsv5453223

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:123

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: 78 SVs from 18 studies. See in: genome view

Submitted genomic10,409,782-10,409,904

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5453223	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	10,409,782	10,409,904
nsv5453223	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	10,549,908	10,550,030

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16910003	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16910003	Submitted genomic		NC_000002.12:g.104 09782_10409904del	GRCh38 (hg38)		NC_000002.12	Chr2	10,409,782	10,409,904
nssv16910003	Remapped	Perfect	NC_000002.11:g.105 49908_10550030del	GRCh37.p13	First Pass	NC_000002.11	Chr2	10,549,908	10,550,030

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)
nssv16910003	<0.001	6	6404

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