A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568839



Internal ID16356248
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 StatusM
Merged Variantsdgv4440n54
Supporting Variantsnssv1149566, nssv1149565, nssv839681, nssv1149564, nssv839682, nssv839680
Samples1780862263_A, NINDS_182, NINDS_31
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568839
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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