A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568614



Internal ID16009337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:26867118..26867902hg38UCSC Ensembl
Innerchr15:27112265..27113049hg19UCSC Ensembl
Innerchr15:24663358..24664142hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38785
hg19785
hg18785
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4398n54
Supporting Variantsnssv839194, nssv839191, nssv839192, nssv839193
Samples
Known GenesGABRA5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568614
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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