A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv471808



Internal ID15561400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42704043..42707508hg38UCSC Ensembl
chr4:42706060..42709525hg19UCSC Ensembl
chr4:42400817..42404282hg18UCSC Ensembl
chr4:42546988..42550453hg17UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg383466
hg193466
hg183466
hg173466
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv646089
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)nsv471808
Frequency
Sample Size95
Observed Gainn/a
Observed Lossn/a
Observed Complexn/a
Frequencyn/a


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