A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593204



Internal ID16033927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:476314..534500hg38UCSC Ensembl
Innerchr4:470103..528289hg19UCSC Ensembl
Innerchr4:460103..518289hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3858187
hg1958187
hg1858187
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153427
SamplesHGDP01405
Known GenesPIGG, ZNF721
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593204
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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