A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv879490



Internal ID6286501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:74268658..74284686hg19UCSC Ensembl
Outerchr4:74258832..74285223hg19UCSC Ensembl
Innerchr4:74487522..74503550hg18UCSC Ensembl
Outerchr4:74477696..74504087hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Gain
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1502647
SamplesSP51307
Known GenesALB
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv879490
Frequency
Sample Size6533
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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