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dbVar

Database of genomic structural variation

nsv4418797

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:603,344

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: 1672 SVs from 83 studies. See in: genome view

Remapped(Score: Perfect):74,225,600-74,828,943

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
nsv4418797	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	74,225,600	74,238,584	74,828,853	74,828,943
nsv4418797	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	73,936,645	73,949,629	74,539,898	74,539,988

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15708771	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
nssv15708771	Remapped	Perfect	NC_000011.10:g.(74 225600_74238584)_( 74828853_74828943) dup	GRCh38.p12	First Pass	NC_000011.10	Chr11	74,225,600	74,238,584	74,828,853	74,828,943
nssv15708771	Submitted genomic		NC_000011.9:g.(739 36645_73949629)_(7 4539898_74539988)d up	GRCh37 (hg19)		NC_000011.9	Chr11	73,936,645	73,949,629	74,539,898	74,539,988

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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