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dbVar

Database of genomic structural variation

nsv6133291

Organism: Homo sapiens

Study:nstd213 (Pham et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:57,217

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

Remapped(Score: Perfect):61,879,839-61,937,055

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv6133291	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000017.11	Chr17	61,879,839	61,879,855	61,937,039	61,937,055
nsv6133291	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000017.10	Chr17	59,957,200	59,957,216	60,014,400	60,014,416

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17679775	deletion	SAMN20524660	Sequencing	Paired-end mapping	208

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv17679775	Remapped	Perfect	NC_000017.11:g.(61 879839_61879855)_( 61937039_61937055) del	GRCh38.p12	First Pass	NC_000017.11	Chr17	61,879,839	61,879,855	61,937,039	61,937,055
nssv17679775	Submitted genomic		NC_000017.10:g.(59 957200_59957216)_( 60014400_60014416) del	GRCh37 (hg19)		NC_000017.10	Chr17	59,957,200	59,957,216	60,014,400	60,014,416

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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