A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv471783



Internal ID15214698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62624900..62626409hg38UCSC Ensembl
chr3:62610575..62612084hg19UCSC Ensembl
chr3:62585615..62587124hg18UCSC Ensembl
chr3:62585615..62587124hg17UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg381510
hg191510
hg181510
hg171510
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv646064
Samples
Known GenesCADPS
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)nsv471783
Frequency
Sample Size95
Observed Gainn/a
Observed Lossn/a
Observed Complexn/a
Frequencyn/a


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