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dbVar

Database of genomic structural variation

nsv5938802

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:283

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: 203 SVs from 25 studies. See in: genome view

Submitted genomic27,044,291-27,044,573

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5938802	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	27,044,291	27,044,573
nsv5938802	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	24,624,255	24,624,537

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17388022	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17388022	Submitted genomic		NC_000018.10:g.270 44291_27044573del	GRCh38 (hg38)		NC_000018.10	Chr18	27,044,291	27,044,573
nssv17388022	Remapped	Perfect	NC_000018.9:g.2462 4255_24624537del	GRCh37.p13	First Pass	NC_000018.9	Chr18	24,624,255	24,624,537

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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