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dbVar

Database of genomic structural variation

nsv5932833

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:67

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: 216 SVs from 23 studies. See in: genome view

Submitted genomic36,055,900-36,055,966

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5932833	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	36,055,900	36,055,966
nsv5932833	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	33,635,863	33,635,929

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17375164	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17375164	Submitted genomic		NC_000018.10:g.360 55900_36055966del	GRCh38 (hg38)		NC_000018.10	Chr18	36,055,900	36,055,966
nssv17375164	Remapped	Perfect	NC_000018.9:g.3363 5863_33635929del	GRCh37.p13	First Pass	NC_000018.9	Chr18	33,635,863	33,635,929

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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