A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152059



Internal ID15877832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:172621962..172680078hg38UCSC Ensembl
Innerchr3:172339752..172397868hg19UCSC Ensembl
Innerchr3:173822446..173880562hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3858117
hg1958117
hg1858117
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592519
Supporting Variants
SamplesHGDP01052
Known GenesNCEH1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152059
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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