A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149563



Internal ID15880830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:31727863..32151722hg38UCSC Ensembl
Innerchr15:32020066..32443923hg19UCSC Ensembl
Innerchr15:29807358..30231215hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38423860
hg19423858
hg18423858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv568838
Supporting Variants
SamplesNINDS_35
Known GenesCHRNA7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149563
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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