A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1674755



Internal ID15185577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:17149143..17299144hg38UCSC Ensembl
Innerchr11:17170690..17320691hg19UCSC Ensembl
Innerchr11:17127266..17277267hg18UCSC Ensembl
Innerchr11:17134999..17285000hg16UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38150002
hg19150002
hg18150002
hg16150002
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469762
Supporting Variants
Samples
Known GenesNUCB2, PIK3C2A
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)nssv1674755
Frequency
Sample Size265
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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