A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469799



Internal ID15534514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:60974823..61116737hg38UCSC Ensembl
Innerchr6:57942570..58084484hg19UCSC Ensembl
Innerchr6:58050529..58192443hg18UCSC Ensembl
Innerchr6:57989406..58131320hg16UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38141915
hg19141915
hg18141915
hg16141915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1672138
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)nsv469799
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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