A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594232



Internal ID16381641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:58574420..58618433hg38UCSC Ensembl
Innerchr4:59440585..59484598hg19UCSC Ensembl
Innerchr4:59135342..59179355hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3844014
hg1944014
hg1844014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv998101
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594232
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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