A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469693



Internal ID15534408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:75388485..75539119hg38UCSC Ensembl
Innerchr3:75437636..75588270hg19UCSC Ensembl
Innerchr3:75520326..75670960hg18UCSC Ensembl
Innerchr3:75358537..75509171hg16UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38150635
hg19150635
hg18150635
hg16150635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1673932, nssv1674097, nssv1676122, nssv1676129, nssv1674499, nssv1676311, nssv1675275, nssv1675408, nssv1673337, nssv1675235, nssv1673015, nssv1672203, nssv1674152, nssv1673945, nssv1673471, nssv1672348
Samples
Known GenesFAM86DP
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)nsv469693
Frequency
Sample Size265
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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