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dbVar

Database of genomic structural variation

nsv4400210

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:863,445

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: 3273 SVs from 98 studies. See in: genome view

Remapped(Score: Perfect):55,552,107-56,415,551

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
nsv4400210	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000007.14	Chr7	55,552,107	55,552,107	56,317,719	56,415,551
nsv4400210	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000007.13	Chr7	55,619,800	55,619,800	56,385,412	56,483,244

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15712487	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
nssv15712487	Remapped	Perfect	NC_000007.14:g.(55 552107_55552107)_( 56317719_56415551) dup	GRCh38.p12	First Pass	NC_000007.14	Chr7	55,552,107	55,552,107	56,317,719	56,415,551
nssv15712487	Submitted genomic		NC_000007.13:g.(55 619800_55619800)_( 56385412_56483244) dup	GRCh37 (hg19)		NC_000007.13	Chr7	55,619,800	55,619,800	56,385,412	56,483,244

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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