A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593786



Internal ID16381195
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 StatusM
Merged Variants
Supporting Variantsnssv993234
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593786
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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