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dbVar

Database of genomic structural variation

nsv5941151

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:851

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: 136 SVs from 30 studies. See in: genome view

Submitted genomic27,615,616-27,616,466

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5941151	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	27,615,616	27,616,466
nsv5941151	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	27,626,937	27,627,787

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17387068	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17387068	Submitted genomic		NC_000016.10:g.276 15616_27616466del	GRCh38 (hg38)		NC_000016.10	Chr16	27,615,616	27,616,466
nssv17387068	Remapped	Perfect	NC_000016.9:g.2762 6937_27627787del	GRCh37.p13	First Pass	NC_000016.9	Chr16	27,626,937	27,627,787

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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