A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv471755



Internal ID15561347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:87722513..87724332hg38UCSC Ensembl
chr11:87433405..87435224hg19UCSC Ensembl
chr11:87111053..87112872hg18UCSC Ensembl
chr11:87111053..87112872hg17UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg381820
hg191820
hg181820
hg171820
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv646036
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)nsv471755
Frequency
Sample Size95
Observed Gainn/a
Observed Lossn/a
Observed Complexn/a
Frequencyn/a


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