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dbVar

Database of genomic structural variation

nsv5938569

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:39,983

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: 273 SVs from 44 studies. See in: genome view

Submitted genomic36,489,086-36,529,068

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5938569	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	36,489,086	36,529,068
nsv5938569	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	36,979,988	37,019,970

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17405263	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17405263	Submitted genomic		NC_000019.10:g.364 89086_36529068del	GRCh38 (hg38)		NC_000019.10	Chr19	36,489,086	36,529,068
nssv17405263	Remapped	Perfect	NC_000019.9:g.3697 9988_37019970del	GRCh37.p13	First Pass	NC_000019.9	Chr19	36,979,988	37,019,970

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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