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dbVar

Database of genomic structural variation

nsv5940253

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:264

Publication(s):Almarri et al. 2020

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: 98 SVs from 26 studies. See in: genome view

Submitted genomic71,468,973-71,469,236

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5940253	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	71,468,973	71,469,236
nsv5940253	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	71,935,690	71,935,953

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17369779	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17369779	Submitted genomic		NC_000014.9:g.7146 8973_71469236del	GRCh38 (hg38)		NC_000014.9	Chr14	71,468,973	71,469,236
nssv17369779	Remapped	Perfect	NC_000014.8:g.7193 5690_71935953del	GRCh37.p13	First Pass	NC_000014.8	Chr14	71,935,690	71,935,953

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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