A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9737n54



Internal ID22777632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43556410..43557303hg38UCSC Ensembl
chr5:43556512..43557405hg19UCSC Ensembl
chr5:43592269..43593162hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38894
hg19894
hg18894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597931, nsv597926, nsv597927, nsv597929
Samples
Known GenesPAIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9737n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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