A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3151n54



Internal ID22771046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:52846209..52847977hg38UCSC Ensembl
chr13:53420344..53422112hg19UCSC Ensembl
chr13:52318345..52320113hg18UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg381769
hg191769
hg181769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv561673, nsv561666, nsv561665, nsv561672, nsv561671, nsv561664
Samples
Known GenesPCDH8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3151n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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