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dbVar

Database of genomic structural variation

nsv5011702

Organism: Homo sapiens

Study:nstd200 (Abel 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:3,981

Publication(s):Abel 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: 107 SVs from 25 studies. See in: genome view

Submitted genomic11,557,761-11,561,746

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5011702	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000019.10	Chr19	11,557,763 (-2, +86)	11,561,743 (-79, +3)
nsv5011702	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000019.9	Chr19	11,668,578 (-2, +86)	11,672,558 (-79, +3)

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16572830	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16572830	Submitted genomic		NC_000019.10:g.(11 557761_11557849)_( 11561664_11561746) del	GRCh38 (hg38)		NC_000019.10	Chr19	11,557,763 (-2, +86)	11,561,743 (-79, +3)
nssv16572830	Remapped	Perfect	NC_000019.9:g.(116 68576_11668664)_(1 1672479_11672561)d el	GRCh37.p13	First Pass	NC_000019.9	Chr19	11,668,578 (-2, +86)	11,672,558 (-79, +3)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv16572830	<0.001	1	29246

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