A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584649



Internal ID16025372
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 StatusM
Merged Variants
Supporting Variantsnssv933573, nssv933574, nssv933575
Samples
Known GenesTRIP12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584649
Frequency
Sample Size17421
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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