A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176087



Internal ID15876353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:69864130..69893386hg38UCSC Ensembl
Innerchr9:72479046..72508302hg19UCSC Ensembl
Innerchr9:71668866..71698122hg18UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3829257
hg1929257
hg1829257
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv614580
Supporting Variants
SamplesHGDP00827
Known GenesC9orf135
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176087
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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