A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv592075



Internal ID16379484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:153456330..153503426hg38UCSC Ensembl
Innerchr3:153174119..153221215hg19UCSC Ensembl
Innerchr3:154656809..154703905hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg3847097
hg1947097
hg1847097
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151813
SamplesHGDP01156
Known GenesC3orf79
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv592075
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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