A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9738n54



Internal ID22777633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43556492..43557103hg38UCSC Ensembl
chr5:43556594..43557205hg19UCSC Ensembl
chr5:43592351..43592962hg18UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg38612
hg19612
hg18612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597928, nsv597930
Samples
Known GenesPAIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9738n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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