A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996197



Internal ID15235057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:182869307..183035390hg38UCSC Ensembl
Innerchr3:182587095..182753178hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38166084
hg19166084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv482968
Supporting Variants
Samples
Known GenesATP11B, DCUN1D1, MCCC1
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996197
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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