A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176088



Internal ID15875579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69864130..69898324hg38UCSC Ensembl
Innerchr9:72479046..72513240hg19UCSC Ensembl
Innerchr9:71668866..71703060hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3834195
hg1934195
hg1834195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614581
Supporting Variants
SamplesHGDP00704
Known GenesC9orf135
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176088
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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