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dbVar

Database of genomic structural variation

nsv5935410

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:276

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: 181 SVs from 51 studies. See in: genome view

Submitted genomic67,731,238-67,731,513

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5935410	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	67,731,238	67,731,513
nsv5935410	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	65,727,354	65,727,629

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17379866	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17379866	Submitted genomic		NC_000017.11:g.677 31238_67731513del	GRCh38 (hg38)		NC_000017.11	Chr17	67,731,238	67,731,513
nssv17379866	Remapped	Perfect	NC_000017.10:g.657 27354_65727629del	GRCh37.p13	First Pass	NC_000017.10	Chr17	65,727,354	65,727,629

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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