A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv568862



Internal ID16356271
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 StatusM
Merged Variants
Supporting Variantsnssv1149577, nssv1149575, nssv1149576, nssv1149578
SamplesHGDP00568, HGDP00575, HGDP00599, HGDP00562
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv568862
Frequency
Sample Size17421
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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