A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469576



Internal ID15187605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149682535..149866144hg38UCSC Ensembl
Innerchr7:149379626..149563233hg19UCSC Ensembl
Innerchr7:149010559..149194166hg18UCSC Ensembl
Innerchr7:148771367..148954974hg16UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38183610
hg19183608
hg18183608
hg16183608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1672452
Samples
Known GenesKRBA1, SSPO, ZNF467, ZNF862
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)nsv469576
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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