A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593202



Internal ID16380611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:421522..503349hg38UCSC Ensembl
Innerchr4:415311..497138hg19UCSC Ensembl
Innerchr4:405311..487138hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3881828
hg1981828
hg1881828
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1153426
SamplesHGDP00975
Known GenesABCA11P, PIGG, ZNF721
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593202
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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