A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568658



Internal ID16009381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:27159610..27164655hg38UCSC Ensembl
Innerchr15:27404757..27409802hg19UCSC Ensembl
Innerchr15:24987503..24992548hg18UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg385046
hg195046
hg185046
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4408n54
Supporting Variantsnssv839284, nssv839285
Samples
Known GenesGABRG3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568658
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer