A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1676036



Internal ID15533544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64476875..64698199hg38UCSC Ensembl
Innerchr9:69489293..69710617hg19UCSC Ensembl
Innerchr9:68779113..69000437hg18UCSC Ensembl
Innerchr9:65619734..65841058hg16UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38221325
hg19221325
hg18221325
hg16221325
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469823
Supporting Variants
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)nssv1676036
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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