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dbVar

Database of genomic structural variation

nsv4404179

Organism: Homo sapiens

Study:nstd174 (DGV Gold Standard)
Variant Type:copy number variation
Method Type:Multiple
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:485,201

Links to Other Resources

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: 1348 SVs from 78 studies. See in: genome view

Remapped(Score: Perfect):59,577,276-60,062,476

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
nsv4404179	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000004.12	Chr4	59,577,276	59,674,578	60,030,106	60,062,476
nsv4404179	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000004.11	Chr4	60,442,994	60,540,296	60,895,824	60,928,194

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15711505	copy number gain	Multiple	Multiple

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv15711505	Remapped	Perfect	NC_000004.12:g.(59 577276_59674578)_( 60030106_60062476) dup	GRCh38.p12	First Pass	NC_000004.12	Chr4	59,577,276	59,674,578	60,030,106	60,062,476
nssv15711505	Submitted genomic		NC_000004.11:g.(60 442994_60540296)_( 60895824_60928194) dup	GRCh37 (hg19)		NC_000004.11	Chr4	60,442,994	60,540,296	60,895,824	60,928,194

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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