A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469530



Internal ID15534245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:85176912..85268905hg38UCSC Ensembl
Innerchr15:85720143..85812136hg19UCSC Ensembl
Innerchr15:83521147..83613140hg18UCSC Ensembl
Innerchr15:83449911..83541904hg16UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3891994
hg1991994
hg1891994
hg1691994
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1674507, nssv1673418, nssv1673637
Samples
Known GenesLOC440300, LOC642423
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)nsv469530
Frequency
Sample Size265
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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