A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4547n54



Internal ID22772442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55363754..55364417hg38UCSC Ensembl
chr15:55655952..55656615hg19UCSC Ensembl
chr15:53443244..53443907hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38664
hg19664
hg18664
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv569537, nsv569538, nsv569536
Samples
Known GenesCCPG1, DYX1C1-CCPG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv4547n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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