A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593203



Internal ID16380612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:432092..482918hg38UCSC Ensembl
Innerchr4:425881..476707hg19UCSC Ensembl
Innerchr4:415881..466707hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3850827
hg1950827
hg1850827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv987408
Samples
Known GenesABCA11P, ZNF721
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593203
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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