A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555966



Internal ID15996689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:94131155..94231751hg38UCSC Ensembl
Innerchr11:93864321..93964917hg19UCSC Ensembl
Innerchr11:93503969..93604565hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38100597
hg19100597
hg18100597
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174906
SamplesHGDP01254
Known GenesPANX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555966
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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