A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469670



Internal ID15187699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:102020338..102186517hg38UCSC Ensembl
InnerchrX:101275311..101441490hg19UCSC Ensembl
InnerchrX:101161967..101328146hg18UCSC Ensembl
InnerchrX:100047168..100213347hg16UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38166180
hg19166180
hg18166180
hg16166180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1673666
Samples
Known GenesBEX5, TCEAL2, TCEAL6
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)nsv469670
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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