A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv646064



Internal ID15214598
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 Flag1
Merged StatusS
Merged Variantsnsv471783
Supporting Variants
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)nssv646064
Frequency
Sample Size95
Observed Gainn/a
Observed Lossn/a
Observed Complexn/a
Frequencyn/a


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