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dbVar

Database of genomic structural variation

nsv5872313

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:60

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: 100 SVs from 24 studies. See in: genome view

Submitted genomic69,656,277-69,656,336

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5872313	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000002.12	Chr2	69,656,277	69,656,336
nsv5872313	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000002.11	Chr2	69,883,409	69,883,468

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17397542	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17397542	Submitted genomic		NC_000002.12:g.696 56277_69656336del	GRCh38 (hg38)		NC_000002.12	Chr2	69,656,277	69,656,336
nssv17397542	Remapped	Perfect	NC_000002.11:g.698 83409_69883468del	GRCh37.p13	First Pass	NC_000002.11	Chr2	69,883,409	69,883,468

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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