A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469619



Internal ID15187648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:73999518..74173980hg38UCSC Ensembl
Innerchr15:74291859..74466321hg19UCSC Ensembl
Innerchr15:72078912..72253374hg18UCSC Ensembl
Innerchr15:72007676..72182138hg16UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38174463
hg19174463
hg18174463
hg16174463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1675928, nssv1674345
Samples
Known GenesGOLGA6A, ISLR, ISLR2, LOC283731, PML
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)nsv469619
Frequency
Sample Size265
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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