A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6n29



Internal ID22767694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:143737005..143935817hg38UCSC Ensembl
chr4:144658158..144856970hg19UCSC Ensembl
chr4:144877608..145076420hg18UCSC Ensembl
chr4:145235785..145434597hg16UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38198813
hg19198813
hg18198813
hg16198813
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv469811, nsv469812
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)dgv6n29
Frequency
Sample Size265
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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