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dbVar

Database of genomic structural variation

nsv5944144

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:256

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: 140 SVs from 33 studies. See in: genome view

Submitted genomic33,081,874-33,082,129

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5944144	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	33,081,874	33,082,129
nsv5944144	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	33,572,780	33,573,035

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17405581	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17405581	Submitted genomic		NC_000019.10:g.330 81874_33082129del	GRCh38 (hg38)		NC_000019.10	Chr19	33,081,874	33,082,129
nssv17405581	Remapped	Perfect	NC_000019.9:g.3357 2780_33573035del	GRCh37.p13	First Pass	NC_000019.9	Chr19	33,572,780	33,573,035

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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