A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1176415



Internal ID15533661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:64997940..65143890hg38UCSC Ensembl
Innerchr12:65391720..65537670hg19UCSC Ensembl
Innerchr12:63677987..63823937hg18UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg38145951
hg19145951
hg18145951
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv559205
Supporting Variants
SamplesNINDS_198
Known GenesWIF1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1176415
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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