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dbVar

Database of genomic structural variation

nsv5598979

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:72

Publication(s):Ebert et al. 2021

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: 97 SVs from 29 studies. See in: genome view

Submitted genomic10,182,391-10,182,462

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5598979	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	10,182,391	10,182,462
nsv5598979	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	10,293,067	10,293,138

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17103112	deletion	SAMN00001694	Sequencing	Sequence alignment	8,610

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17103112	Submitted genomic		NC_000019.10:g.101 82391_10182462delA	GRCh38 (hg38)		NC_000019.10	Chr19	10,182,391	10,182,462
nssv17103112	Remapped	Perfect	NC_000019.9:g.1029 3067_10293138delA	GRCh37.p13	First Pass	NC_000019.9	Chr19	10,293,067	10,293,138

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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