A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176086



Internal ID15528131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69485202..69517283hg38UCSC Ensembl
Innerchr9:72100118..72132199hg19UCSC Ensembl
Innerchr9:71289938..71322019hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3832082
hg1932082
hg1832082
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614578
Supporting Variants
SamplesHGDP00594
Known GenesAPBA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176086
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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