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dbVar

Database of genomic structural variation

nsv5517005

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:2,958

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: 124 SVs from 27 studies. See in: genome view

Submitted genomic4,937,505-4,940,462

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5517005	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	4,937,505	4,940,462
nsv5517005	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	4,937,517	4,940,474

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17720788	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17720788	Submitted genomic		NC_000019.10:g.493 7505_4940462del	GRCh38 (hg38)		NC_000019.10	Chr19	4,937,505	4,940,462
nssv17720788	Remapped	Perfect	NC_000019.9:g.4937 517_4940474del	GRCh37.p13	First Pass	NC_000019.9	Chr19	4,937,517	4,940,474

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)
nssv17720788	<0.001	6	6404

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