A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593760



Internal ID16381169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15001808..15005133hg38UCSC Ensembl
Innerchr4:15003432..15006757hg19UCSC Ensembl
Innerchr4:14612530..14615855hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg383326
hg193326
hg183326
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv993084
Samples
Known GenesCPEB2, CPEB2-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593760
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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