A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593191



Internal ID16033914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:79447..122443hg38UCSC Ensembl
Innerchr4:79340..122323hg19UCSC Ensembl
Innerchr4:69340..112323hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3842997
hg1942984
hg1842984
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv987399
Samples
Known GenesZNF595, ZNF718
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593191
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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