A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469736



Internal ID15534451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:264407..434413hg38UCSC Ensembl
Innerchr4:258196..428202hg19UCSC Ensembl
Innerchr4:248196..418202hg18UCSC Ensembl
Innerchr4:248196..418202hg16UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38170007
hg19170007
hg18170007
hg16170007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1676064, nssv1672279, nssv1673102, nssv1675345, nssv1676072
Samples
Known GenesABCA11P, ZNF141, ZNF732
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)nsv469736
Frequency
Sample Size265
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer