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dbVar

Database of genomic structural variation

nsv5498788

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:70

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

Submitted genomic34,790,864-34,790,933

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5498788	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	34,790,864	34,790,933
nsv5498788	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	35,260,070	35,260,139

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17696867	duplication	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17696867	Submitted genomic		NC_000014.9:g.3479 0864_34790933dup	GRCh38 (hg38)		NC_000014.9	Chr14	34,790,864	34,790,933
nssv17696867	Remapped	Perfect	NC_000014.8:g.3526 0070_35260139dup	GRCh37.p13	First Pass	NC_000014.8	Chr14	35,260,070	35,260,139

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)
nssv17696867	<0.001	1	6404

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