A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568835



Internal ID16356244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31727716..32151995hg38UCSC Ensembl
Innerchr15:32019919..32444196hg19UCSC Ensembl
Innerchr15:29807211..30231488hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38424280
hg19424278
hg18424278
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4440n54
Supporting Variantsnssv1149561, nssv1149560, nssv1149559, nssv1149558, nssv1149562, nssv839669
SamplesHGDP00570, HGDP00148, HGDP00474, HGDP00594, HGDP00564
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568835
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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