A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175091



Internal ID15532388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:43897861..43927961hg38UCSC Ensembl
Innerchr11:43919411..43949511hg19UCSC Ensembl
Innerchr11:43875987..43906087hg18UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3830101
hg1930101
hg1830101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554171
Supporting Variants
SamplesHGDP01303
Known GenesALKBH3, ALKBH3-AS1, SEC14L1P1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175091
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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