A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10095n54



Internal ID22777990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140846323..140864165hg38UCSC Ensembl
chr5:140225908..140243750hg19UCSC Ensembl
chr5:140206092..140223934hg18UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3817843
hg1917843
hg1817843
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv599849, nsv599850
Samples
Known GenesPCDHA1, PCDHA10, PCDHA2, PCDHA3, PCDHA4, PCDHA5, PCDHA6, PCDHA7, PCDHA8, PCDHA9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10095n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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