A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469811



Internal ID15534526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143737005..143903378hg38UCSC Ensembl
Innerchr4:144658158..144824531hg19UCSC Ensembl
Innerchr4:144877608..145043981hg18UCSC Ensembl
Innerchr4:145235785..145402158hg16UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38166374
hg19166374
hg18166374
hg16166374
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6n29
Supporting Variantsnssv1673903, nssv1673492, nssv1674370, nssv1675079, nssv1674440, nssv1675358
Samples
Known GenesGYPE
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)nsv469811
Frequency
Sample Size265
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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