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dbVar

Database of genomic structural variation

nsv5505902

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:117

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: 60 SVs from 15 studies. See in: genome view

Submitted genomic23,301,429-23,301,545

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5505902	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	23,301,429	23,301,545
nsv5505902	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	23,770,638	23,770,754

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17693969	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17693969	Submitted genomic		NC_000014.9:g.2330 1429_23301545dup	GRCh38 (hg38)		NC_000014.9	Chr14	23,301,429	23,301,545
nssv17693969	Remapped	Perfect	NC_000014.8:g.2377 0638_23770754dup	GRCh37.p13	First Pass	NC_000014.8	Chr14	23,770,638	23,770,754

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)
nssv17693969	0.004	26	6404

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