A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv469807



Internal ID15187836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:79043070..79212669hg38UCSC Ensembl
Innerchr10:80802827..80972426hg19UCSC Ensembl
Innerchr10:80472833..80642432hg18UCSC Ensembl
Innerchr10:80147430..80317029hg16UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38169600
hg19169600
hg18169600
hg16169600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1674270, nssv1675183, nssv1675346, nssv1672364, nssv1675002
Samples
Known GenesZMIZ1, ZMIZ1-AS1
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)nsv469807
Frequency
Sample Size265
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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