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dbVar

Database of genomic structural variation

nsv5931879

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:122

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: 164 SVs from 35 studies. See in: genome view

Submitted genomic66,587,663-66,587,784

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5931879	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	66,587,663	66,587,784
nsv5931879	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	64,583,781	64,583,902

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17384199	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17384199	Submitted genomic		NC_000017.11:g.665 87663_66587784del	GRCh38 (hg38)		NC_000017.11	Chr17	66,587,663	66,587,784
nssv17384199	Remapped	Perfect	NC_000017.10:g.645 83781_64583902del	GRCh37.p13	First Pass	NC_000017.10	Chr17	64,583,781	64,583,902

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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