A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv933574



Internal ID15880844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:229731636..229899510hg38UCSC Ensembl
Innerchr2:230596352..230764226hg19UCSC Ensembl
Innerchr2:230304596..230472470hg18UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38167875
hg19167875
hg18167875
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584649
Supporting Variants
Samples
Known GenesTRIP12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv933574
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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