A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv989311



Internal ID16283267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5184198..5593242hg38UCSC Ensembl
Innerchr4:5185925..5594969hg19UCSC Ensembl
Innerchr4:5236826..5645870hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38409045
hg19409045
hg18409045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593482
Supporting Variants
Samples
Known GenesC4orf6, EVC2, STK32B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv989311
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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