A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593488



Internal ID16380897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5455067..5490421hg38UCSC Ensembl
Innerchr4:5456794..5492148hg19UCSC Ensembl
Innerchr4:5507695..5543049hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3835355
hg1935355
hg1835355
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv989314
Samples
Known GenesSTK32B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593488
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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