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dbVar

Database of genomic structural variation

nsv5924292

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:133

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: 105 SVs from 28 studies. See in: genome view

Submitted genomic122,185,417-122,185,549

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5924292	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	122,185,417	122,185,549
nsv5924292	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	124,947,696	124,947,828

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17431921	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17431921	Submitted genomic		NC_000009.12:g.122 185417_122185549de l	GRCh38 (hg38)		NC_000009.12	Chr9	122,185,417	122,185,549
nssv17431921	Remapped	Perfect	NC_000009.11:g.124 947696_124947828de l	GRCh37.p13	First Pass	NC_000009.11	Chr9	124,947,696	124,947,828

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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