A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469525



Internal ID15534240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:14801735..14966209hg38UCSC Ensembl
Innerchr2:14941859..15106333hg19UCSC Ensembl
Innerchr2:14859310..15023784hg18UCSC Ensembl
Innerchr2:14963598..15128072hg16UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38164475
hg19164475
hg18164475
hg16164475
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1675583
Samples
Known Genes
MethodBAC aCGH
AnalysisA locus was considered a CNV if the log ratio of fluorescence measurements for the individuals assayed exceeded twice the SD of the autosomal clones in both dye-swapped experiments.
PlatformGPL4010
Comments
ReferenceLocke_et_al_2006
Pubmed ID16826518
Accession Number(s)nsv469525
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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