A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593190



Internal ID16033913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:73616..288710hg38UCSC Ensembl
Innerchr4:73508..282499hg19UCSC Ensembl
Innerchr4:63508..272499hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38215095
hg19208992
hg18208992
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv987398
Samples
Known GenesZNF595, ZNF718, ZNF732, ZNF876P
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593190
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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