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dbVar

Database of genomic structural variation

nsv5937672

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:144,766

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: 564 SVs from 66 studies. See in: genome view

Submitted genomic38,548,476-38,693,241

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5937672	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	38,548,476	38,693,241
nsv5937672	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	39,039,116	39,183,881

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17396186	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17396186	Submitted genomic		NC_000019.10:g.385 48476_38693241del	GRCh38 (hg38)		NC_000019.10	Chr19	38,548,476	38,693,241
nssv17396186	Remapped	Perfect	NC_000019.9:g.3903 9116_39183881del	GRCh37.p13	First Pass	NC_000019.9	Chr19	39,039,116	39,183,881

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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