A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv993234



Internal ID16287190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:19487248..19708172hg38UCSC Ensembl
Innerchr4:19488871..19709795hg19UCSC Ensembl
Innerchr4:19097969..19318893hg18UCSC Ensembl
Cytoband4p15.31
Allele length
AssemblyAllele length
hg38220925
hg19220925
hg18220925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593786
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv993234
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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