A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469678



Internal ID15534393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28555639..28719643hg38UCSC Ensembl
Innerchr15:28800785..28964789hg19UCSC Ensembl
Innerchr15:26599826..26763830hg18UCSC Ensembl
Innerchr15:26528590..26692594hg16UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38164005
hg19164005
hg18164005
hg16164005
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1673445
Samples
Known GenesGOLGA8M, HERC2P9
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)nsv469678
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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