A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176144



Internal ID15528024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:114048610..114104774hg38UCSC Ensembl
Innerchr9:116810890..116867054hg19UCSC Ensembl
Innerchr9:115850711..115906875hg18UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3856165
hg1956165
hg1856165
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615222
Supporting Variants
SamplesHGDP00578
Known GenesAMBP, KIF12, ZNF618
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176144
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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