A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1676141



Internal ID15533649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:857757..1001369hg38UCSC Ensembl
Innerchr17:760997..904609hg19UCSC Ensembl
Innerchr17:707747..851359hg18UCSC Ensembl
Innerchr17:745747..889359hg16UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38143613
hg19143613
hg18143613
hg16143613
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469582
Supporting Variants
Samples
Known GenesNXN, TIMM22
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)nssv1676141
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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