A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555187



Internal ID15995910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:64185649..64260416hg38UCSC Ensembl
Innerchr11:63953121..64027888hg19UCSC Ensembl
Innerchr11:63709697..63784464hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3874768
hg1974768
hg1874768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv777149
Samples
Known GenesDNAJC4, FERMT3, FKBP2, NUDT22, PLCB3, PPP1R14B, STIP1, TRPT1, VEGFB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555187
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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