A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149566



Internal ID15880259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31727863..32151995hg38UCSC Ensembl
Innerchr15:32020066..32444196hg19UCSC Ensembl
Innerchr15:29807358..30231488hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38424133
hg19424131
hg18424131
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568839
Supporting Variants
SamplesNINDS_182
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149566
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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