A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568817



Internal ID16356226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31483399..31484300hg38UCSC Ensembl
Innerchr15:31775602..31776503hg19UCSC Ensembl
Innerchr15:29562894..29563795hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38902
hg19902
hg18902
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4437n54
Supporting Variantsnssv839630, nssv839636, nssv839637, nssv839645, nssv839639, nssv839640, nssv839646, nssv839638, nssv839643, nssv839641, nssv839644, nssv839632, nssv839635, nssv839642, nssv839633, nssv839634, nssv839631
Samples
Known GenesOTUD7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568817
Frequency
Sample Size17421
Observed Gain12
Observed Loss5
Observed Complex0
Frequencyn/a


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