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dbVar

Database of genomic structural variation

nsv5919426

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:80

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: 221 SVs from 34 studies. See in: genome view

Submitted genomic166,955,255-166,955,334

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5919426	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	166,955,255	166,955,334
nsv5919426	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	167,368,743	167,368,822

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17410138	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17410138	Submitted genomic		NC_000006.12:g.166 955255_166955334de l	GRCh38 (hg38)		NC_000006.12	Chr6	166,955,255	166,955,334
nssv17410138	Remapped	Perfect	NC_000006.11:g.167 368743_167368822de l	GRCh37.p13	First Pass	NC_000006.11	Chr6	167,368,743	167,368,822

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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