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dbVar

Database of genomic structural variation

nsv5923857

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:71

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: 210 SVs from 31 studies. See in: genome view

Submitted genomic166,449,812-166,449,882

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5923857	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	166,449,812	166,449,882
nsv5923857	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	166,863,300	166,863,370

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17417840	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17417840	Submitted genomic		NC_000006.12:g.166 449812_166449882de l	GRCh38 (hg38)		NC_000006.12	Chr6	166,449,812	166,449,882
nssv17417840	Remapped	Perfect	NC_000006.11:g.166 863300_166863370de l	GRCh37.p13	First Pass	NC_000006.11	Chr6	166,863,300	166,863,370

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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