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dbVar

Database of genomic structural variation

nsv4409411

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:223,798

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: 732 SVs from 64 studies. See in: genome view

Remapped(Score: Perfect):76,895,111-77,118,908

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
nsv4409411	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000005.10	Chr5	76,895,111	76,928,101	77,105,685	77,118,908
nsv4409411	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000005.9	Chr5	76,190,936	76,223,926	76,401,510	76,414,733

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15711928	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
nssv15711928	Remapped	Perfect	NC_000005.10:g.(76 895111_76928101)_( 77105685_77118908) dup	GRCh38.p12	First Pass	NC_000005.10	Chr5	76,895,111	76,928,101	77,105,685	77,118,908
nssv15711928	Submitted genomic		NC_000005.9:g.(761 90936_76223926)_(7 6401510_76414733)d up	GRCh37 (hg19)		NC_000005.9	Chr5	76,190,936	76,223,926	76,401,510	76,414,733

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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