A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv471718



Internal ID15561410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80162940..80163143hg38UCSC Ensembl
chr16:80196837..80197040hg19UCSC Ensembl
chr16:78754338..78754541hg18UCSC Ensembl
chr16:78754338..78754541hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38204
hg19204
hg18204
hg17204
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv645999
Samples
Known Genes
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)nsv471718
Frequency
Sample Size95
Observed Gainn/a
Observed Lossn/a
Observed Complexn/a
Frequencyn/a


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