A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv646053



Internal ID15561273
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 Flag1
Merged StatusS
Merged Variantsnsv471772
Supporting Variants
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)nssv646053
Frequency
Sample Size95
Observed Gainn/a
Observed Lossn/a
Observed Complexn/a
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer