A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568849



Internal ID16356258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31841775..32151995hg38UCSC Ensembl
Innerchr15:32133978..32444196hg19UCSC Ensembl
Innerchr15:29921270..30231488hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38310221
hg19310219
hg18310219
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4442n54
Supporting Variantsnssv839691, nssv839690, nssv839693, nssv839692
Samples
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568849
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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