A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1673821



Internal ID15184643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:40971215..41124330hg38UCSC Ensembl
Innerchr9:69044444..69197559hg19UCSC Ensembl
Innerchr9:68334264..68487379hg18UCSC Ensembl
Innerchr9:65370528..65523634hg16UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38153116
hg19153116
hg18153116
hg16153107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469684
Supporting Variants
Samples
Known GenesLOC440896, PGM5P2
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)nssv1673821
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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