A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9497n54



Internal ID22777392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:668222..699075hg38UCSC Ensembl
chr5:668337..699190hg19UCSC Ensembl
chr5:721337..752190hg18UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg3830854
hg1930854
hg1830854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv596716, nsv596715, nsv596713
Samples
Known GenesTPPP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9497n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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