A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv471771



Internal ID15214686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19434896..19435117hg38UCSC Ensembl
chr1:19761390..19761611hg19UCSC Ensembl
chr1:19633977..19634198hg18UCSC Ensembl
chr1:19506696..19506917hg17UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38222
hg19222
hg18222
hg17222
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv646052
Samples
Known GenesCAPZB
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)nsv471771
Frequency
Sample Size95
Observed Gainn/a
Observed Lossn/a
Observed Complexn/a
Frequencyn/a


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