A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556135



Internal ID16343544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:101528779..101565958hg38UCSC Ensembl
Innerchr11:101399510..101436689hg19UCSC Ensembl
Innerchr11:100904720..100941899hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3837180
hg1937180
hg1837180
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2132n54
Supporting Variantsnssv781999
Samples
Known GenesTRPC6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556135
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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