A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1673430



Internal ID15184252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46173040..46325342hg38UCSC Ensembl
Innerchr10:47544276..47696578hg19UCSC Ensembl
Innerchr10:47014282..47166584hg18UCSC Ensembl
Innerchr10:46859266..47011568hg16UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38152303
hg19152303
hg18152303
hg16152303
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469676
Supporting Variants
Samples
Known GenesANTXRL, ANTXRLP1
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)nssv1673430
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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