A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1674720



Internal ID15185542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:135112233..135264658hg38UCSC Ensembl
InnerchrX:134246263..134398604hg19UCSC Ensembl
InnerchrX:134073929..134226270hg18UCSC Ensembl
InnerchrX:132951870..133104211hg16UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38152426
hg19152342
hg18152342
hg16152342
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469825
Supporting Variants
Samples
Known GenesCXorf48, LINC00633, LOC100287728
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)nssv1674720
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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