A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3152n54



Internal ID22771047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52846209..52848312hg38UCSC Ensembl
chr13:53420344..53422447hg19UCSC Ensembl
chr13:52318345..52320448hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg382104
hg192104
hg182104
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv561670, nsv561668
Samples
Known GenesPCDH8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3152n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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