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dbVar

Database of genomic structural variation

nsv5897832

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:331

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: 308 SVs from 56 studies. See in: genome view

Submitted genomic37,293,697-37,294,027

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5897832	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	37,293,697	37,294,027
nsv5897832	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	37,293,799	37,294,129

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17423460	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17423460	Submitted genomic		NC_000005.10:g.372 93697_37294027del	GRCh38 (hg38)		NC_000005.10	Chr5	37,293,697	37,294,027
nssv17423460	Remapped	Perfect	NC_000005.9:g.3729 3799_37294129del	GRCh37.p13	First Pass	NC_000005.9	Chr5	37,293,799	37,294,129

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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