A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1175735



Internal ID15526534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:91111068..91258928hg38UCSC Ensembl
Innerchr12:91504845..91652705hg19UCSC Ensembl
Innerchr12:90028976..90176836hg18UCSC Ensembl
Cytoband12q21.33
Allele length
AssemblyAllele length
hg38147861
hg19147861
hg18147861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559753
Supporting Variants
SamplesHGDP00145
Known GenesDCN, LUM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1175735
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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