A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593759



Internal ID16381168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15001808..15004089hg38UCSC Ensembl
Innerchr4:15003432..15005713hg19UCSC Ensembl
Innerchr4:14612530..14614811hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382282
hg192282
hg182282
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv993083
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)nsv593759
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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