A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9586n54



Internal ID22777481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:12765180..12892253hg38UCSC Ensembl
chr5:12765292..12892365hg19UCSC Ensembl
chr5:12818292..12945365hg18UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38127074
hg19127074
hg18127074
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv597167, nsv597171
Samples
Known GenesCT49
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9586n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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