A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv993082



Internal ID16287038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:15001808..15003839hg38UCSC Ensembl
Innerchr4:15003432..15005463hg19UCSC Ensembl
Innerchr4:14612530..14614561hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382032
hg192032
hg182032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv593758
Supporting Variants
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)nssv993082
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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