A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469728



Internal ID15534443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64463707..64649709hg38UCSC Ensembl
Innerchr9:69476125..69662127hg19UCSC Ensembl
Innerchr9:68765945..68951947hg18UCSC Ensembl
Innerchr9:65606566..65792568hg16UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38186003
hg19186003
hg18186003
hg16186003
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1675280, nssv1673597, nssv1675039, nssv1673616, nssv1676016, nssv1672387, nssv1676333
Samples
Known GenesLOC100133920
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)nsv469728
Frequency
Sample Size265
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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