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dbVar

Database of genomic structural variation

nsv6132763

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:148,748

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: 451 SVs from 47 studies. See in: genome view

Remapped(Score: Perfect):29,587,913-29,736,660

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
nsv6132763	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000014.9	Chr14	29,587,913	29,587,930	29,736,641	29,736,660
nsv6132763	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000014.8	Chr14	30,057,119	30,057,136	30,205,847	30,205,866

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17681793	duplication	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
nssv17681793	Remapped	Perfect	NC_000014.9:g.(295 87913_29587930)_(2 9736641_29736660)d up	GRCh38.p12	First Pass	NC_000014.9	Chr14	29,587,913	29,587,930	29,736,641	29,736,660
nssv17681793	Submitted genomic		NC_000014.8:g.(300 57119_30057136)_(3 0205847_30205866)d up	GRCh37 (hg19)		NC_000014.8	Chr14	30,057,119	30,057,136	30,205,847	30,205,866

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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