A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996196



Internal ID15235056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:48597171..48770835hg38UCSC Ensembl
Innerchr13:49171307..49344971hg19UCSC Ensembl
Cytoband13q14.2
Allele length
AssemblyAllele length
hg38173665
hg19173665
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483118
Supporting Variants
Samples
Known GenesCYSLTR2
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2996196
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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