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dbVar

Database of genomic structural variation

nsv5944733

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:2,751

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: 172 SVs from 18 studies. See in: genome view

Submitted genomic21,389,118-21,391,868

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5944733	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000018.10	Chr18	21,389,118	21,391,868
nsv5944733	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000018.9	Chr18	18,969,079	18,971,829

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17379222	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17379222	Submitted genomic		NC_000018.10:g.213 89118_21391868del	GRCh38 (hg38)		NC_000018.10	Chr18	21,389,118	21,391,868
nssv17379222	Remapped	Perfect	NC_000018.9:g.1896 9079_18971829del	GRCh37.p13	First Pass	NC_000018.9	Chr18	18,969,079	18,971,829

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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