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dbVar

Database of genomic structural variation

nsv5488083

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:55

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: 87 SVs from 22 studies. See in: genome view

Submitted genomic44,885,764-44,885,818

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5488083	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	44,885,764	44,885,818
nsv5488083	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	44,925,363	44,925,417

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16995531	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16995531	Submitted genomic		NC_000007.14:g.448 85764_44885818del	GRCh38 (hg38)		NC_000007.14	Chr7	44,885,764	44,885,818
nssv16995531	Remapped	Perfect	NC_000007.13:g.449 25363_44925417del	GRCh37.p13	First Pass	NC_000007.13	Chr7	44,925,363	44,925,417

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)
nssv16995531	<0.001	2	6404

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