A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469676



Internal ID15187705
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 gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1676418, nssv1672709, nssv1674916, nssv1673584, nssv1672505, nssv1674765, nssv1672827, nssv1673430, nssv1674890, nssv1675553, nssv1673351
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)nsv469676
Frequency
Sample Size265
Observed Gain7
Observed Loss4
Observed Complex0
Frequencyn/a


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