A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv839657



Internal ID15786927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31625071..32042753hg38UCSC Ensembl
Innerchr15:31917274..32334956hg19UCSC Ensembl
Innerchr15:29704566..30122248hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38417683
hg19417683
hg18417683
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568825
Supporting Variants
Samples
Known GenesCHRNA7, OTUD7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv839657
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