A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552887



Internal ID15993610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:841284..876755hg38UCSC Ensembl
Innerchr11:841284..876755hg19UCSC Ensembl
Innerchr11:831284..866755hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3835472
hg1935472
hg1835472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763585
Samples
Known GenesCHID1, POLR2L, TSPAN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552887
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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