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dbVar

Database of genomic structural variation

nsv5931394

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:1,197

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

Submitted genomic36,520,619-36,521,815

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5931394	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	36,520,619	36,521,815
nsv5931394	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	37,011,521	37,012,717

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17404332	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17404332	Submitted genomic		NC_000019.10:g.365 20619_36521815del	GRCh38 (hg38)		NC_000019.10	Chr19	36,520,619	36,521,815
nssv17404332	Remapped	Perfect	NC_000019.9:g.3701 1521_37012717del	GRCh37.p13	First Pass	NC_000019.9	Chr19	37,011,521	37,012,717

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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