A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1673803



Internal ID15531311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:28199570..28414161hg38UCSC Ensembl
Innerchr15:28444716..28659307hg19UCSC Ensembl
Innerchr15:26118311..26332902hg18UCSC Ensembl
Innerchr15:26047075..26261666hg16UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg38214592
hg19214592
hg18214592
hg16214592
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469883
Supporting Variants
Samples
Known GenesGOLGA8F, GOLGA8G, HERC2
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)nssv1673803
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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