A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8978n54



Internal ID22776873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:15002329..15005183hg38UCSC Ensembl
chr4:15003953..15006807hg19UCSC Ensembl
chr4:14613051..14615905hg18UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg382855
hg192855
hg182855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593764, nsv593768, nsv593767
Samples
Known GenesCPEB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8978n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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