A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv471734



Internal ID15214649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:132422364..132423474hg38UCSC Ensembl
chr2:133179937..133181047hg19UCSC Ensembl
chr2:132896407..132897517hg18UCSC Ensembl
chr2:133013669..133014779hg17UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg381111
hg191111
hg181111
hg171111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv646015
Samples
Known GenesGPR39
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)nsv471734
Frequency
Sample Size95
Observed Gainn/a
Observed Lossn/a
Observed Complexn/a
Frequencyn/a


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