A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1125844



Internal ID15632344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:108998..318153hg38UCSC Ensembl
Innerchr9:108998..318153hg19UCSC Ensembl
Innerchr9:98998..308153hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38209156
hg19209156
hg18209156
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612984
Supporting Variants
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1125844
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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