A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149577



Internal ID15874698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32081490..32151995hg38UCSC Ensembl
Innerchr15:32373693..32444196hg19UCSC Ensembl
Innerchr15:30160985..30231488hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg3870506
hg1970504
hg1870504
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568862
Supporting Variants
SamplesHGDP00575
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149577
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