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dbVar

Database of genomic structural variation

nsv5423876

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:12,641,384

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: 10655 SVs from 64 studies. See in: genome view

Submitted genomic9,108,931-21,750,314

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5423876	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000024.10	ChrY	9,108,931	21,750,314
nsv5423876	Remapped	Pass	GRCh37.p13	Primary Assembly	First Pass	NC_000024.9	ChrY	8,964,956	23,901,428

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17738331	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17738331	Submitted genomic		NC_000024.10:g.910 8931_21750314del	GRCh38 (hg38)		NC_000024.10	ChrY	9,108,931	21,750,314
nssv17738331	Remapped	Pass	NC_000024.9:g.8964 956_23901428del	GRCh37.p13	First Pass	NC_000024.9	ChrY	8,964,956	23,901,428

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)
nssv17738331	0.001	2	1599

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