A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv471772



Internal ID15561364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25084396..25084567hg38UCSC Ensembl
chr1:25410887..25411058hg19UCSC Ensembl
chr1:25283474..25283645hg18UCSC Ensembl
chr1:25156193..25156364hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38172
hg19172
hg18172
hg17172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv646053
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)nsv471772
Frequency
Sample Size95
Observed Gainn/a
Observed Lossn/a
Observed Complexn/a
Frequencyn/a


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