A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv901039



Internal ID6262966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:113439586..114030344hg19UCSC Ensembl
Outerchr13:113436428..114034441hg19UCSC Ensembl
Innerchr13:112487587..113078345hg18UCSC Ensembl
Outerchr13:112484429..113082442hg18UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1589102
SamplesIS38293
Known GenesATP11A, CUL4A, F10, F7, GRTP1, LAMP1, MCF2L, MCF2L-AS1, PCID2, PROZ
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv901039
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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