A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568837



Internal ID16356246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31727716..32240135hg38UCSC Ensembl
Innerchr15:32019919..32532336hg19UCSC Ensembl
Innerchr15:29807211..30319628hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38512420
hg19512418
hg18512418
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4440n54
Supporting Variantsnssv839676, nssv839677, nssv839679, nssv839675, nssv839678
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568837
Frequency
Sample Size17421
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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