A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1675720



Internal ID15533228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:150070986..150220406hg38UCSC Ensembl
Innerchr2:150927500..151076920hg19UCSC Ensembl
Innerchr2:150635746..150785166hg18UCSC Ensembl
Innerchr2:151130045..151279465hg16UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg38149421
hg19149421
hg18149421
hg16149421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv469524
Supporting Variants
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)nssv1675720
Frequency
Sample Size265
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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