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dbVar

Database of genomic structural variation

nsv5917264

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:182

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

Submitted genomic166,304,477-166,304,658

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5917264	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	166,304,477	166,304,658
nsv5917264	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	166,717,965	166,718,146

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17409964	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17409964	Submitted genomic		NC_000006.12:g.166 304477_166304658de l	GRCh38 (hg38)		NC_000006.12	Chr6	166,304,477	166,304,658
nssv17409964	Remapped	Perfect	NC_000006.11:g.166 717965_166718146de l	GRCh37.p13	First Pass	NC_000006.11	Chr6	166,717,965	166,718,146

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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