A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv471760



Internal ID15561352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:73875468..73875644hg38UCSC Ensembl
chr8:74787703..74787879hg19UCSC Ensembl
chr8:74950257..74950433hg18UCSC Ensembl
chr8:74950257..74950433hg17UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg38177
hg19177
hg18177
hg17177
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv646041
Samples
Known GenesUBE2W
MethodOligo aCGH
AnalysisHaploid hybridization data was used to identify genomic intervals showing reduced hybridization signal in comparison to the reference human genome sequence.
PlatformCustom Perlegen arrays
Comments
ReferenceHinds_et_al_2006
Pubmed ID16327809
Accession Number(s)nsv471760
Frequency
Sample Size95
Observed Gainn/a
Observed Lossn/a
Observed Complexn/a
Frequencyn/a


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