A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568864



Internal ID16009587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32151995..32441692hg38UCSC Ensembl
Innerchr15:32444196..32733893hg19UCSC Ensembl
Innerchr15:30231488..30521185hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38289698
hg19289698
hg18289698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv839713
Samples
Known GenesCHRNA7, GOLGA8K, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568864
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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