A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8976n54



Internal ID22776871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15002272..15005183hg38UCSC Ensembl
chr4:15003896..15006807hg19UCSC Ensembl
chr4:14612994..14615905hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382912
hg192912
hg182912
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593761, nsv593766
Samples
Known GenesCPEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8976n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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