A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv10011n54



Internal ID22777906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:113627593..113646953hg38UCSC Ensembl
chr5:112963290..112982650hg19UCSC Ensembl
chr5:112991189..113010549hg18UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg3819361
hg1919361
hg1819361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv599405, nsv599406, nsv599402, nsv599404, nsv599401
SamplesHGDP00722, HGDP00642
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv10011n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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