A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469706



Internal ID15534421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:78655013..78811830hg38UCSC Ensembl
Innerchr10:80414770..80571587hg19UCSC Ensembl
Innerchr10:80084776..80241593hg18UCSC Ensembl
Innerchr10:79759373..79916190hg16UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38156818
hg19156818
hg18156818
hg16156818
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1672271, nssv1676572, nssv1672083, nssv1672837, nssv1673593, nssv1675133, nssv1672537, nssv1675143, nssv1674294, nssv1675027, nssv1675017, nssv1673387, nssv1676580, nssv1675874, nssv1672064, nssv1676447
Samples
Known Genes
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)nsv469706
Frequency
Sample Size265
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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