A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593483



Internal ID16380892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5201075..5434863hg38UCSC Ensembl
Innerchr4:5202802..5436590hg19UCSC Ensembl
Innerchr4:5253703..5487491hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38233789
hg19233789
hg18233789
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv989312
Samples
Known GenesSTK32B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593483
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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