A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175753



Internal ID15530121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125214846..125254077hg38UCSC Ensembl
Innerchr11:125084742..125123973hg19UCSC Ensembl
Innerchr11:124589952..124629183hg18UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3839232
hg1939232
hg1839232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556524
Supporting Variants
SamplesHGDP00897
Known GenesPKNOX2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175753
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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