A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv471766



Internal ID15214681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:86055234..86058799hg38UCSC Ensembl
chr4:86976387..86979952hg19UCSC Ensembl
chr4:87195411..87198976hg18UCSC Ensembl
chr4:87333566..87337131hg17UCSC Ensembl
Cytoband4q21.3
Allele length
AssemblyAllele length
hg383566
hg193566
hg183566
hg173566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv646047
Samples
Known GenesMAPK10
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)nsv471766
Frequency
Sample Size95
Observed Gainn/a
Observed Lossn/a
Observed Complexn/a
Frequencyn/a


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