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dbVar

Database of genomic structural variation

nsv5877871

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:1,937

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

Submitted genomic95,270,633-95,272,569

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5877871	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	95,270,633	95,272,569
nsv5877871	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	95,936,381	95,938,317

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17408647	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17408647	Submitted genomic		NC_000002.12:g.952 70633_95272569del	GRCh38 (hg38)		NC_000002.12	Chr2	95,270,633	95,272,569
nssv17408647	Remapped	Perfect	NC_000002.11:g.959 36381_95938317del	GRCh37.p13	First Pass	NC_000002.11	Chr2	95,936,381	95,938,317

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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