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dbVar

Database of genomic structural variation

nsv5849115

Organism: Homo sapiens

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

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:2,433

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: 112 SVs from 21 studies. See in: genome view

Submitted genomic94,496,614-94,499,046

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5849115	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000014.9	Chr14	94,496,614	94,499,046
nsv5849115	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000014.8	Chr14	94,962,951	94,965,383

Variant Call Information

Variant Call ID	Type	Method	Analysis	Copy number
nssv17470140	copy number variation	Sequencing	Sequence alignment	0
nssv17470141	copy number variation	Sequencing	Sequence alignment	2

Variant Call Placement Information

Variant Call ID	Placement Type	Score	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17470140	Submitted genomic		GRCh38 (hg38)		NC_000014.9	Chr14	94,496,614	94,499,046
nssv17470141	Submitted genomic		GRCh38 (hg38)		NC_000014.9	Chr14	94,496,614	94,499,046
nssv17470140	Remapped	Perfect	GRCh37.p13	First Pass	NC_000014.8	Chr14	94,962,951	94,965,383
nssv17470141	Remapped	Perfect	GRCh37.p13	First Pass	NC_000014.8	Chr14	94,962,951	94,965,383

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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