A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247812



Internal ID21308626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32179286..32520328hg38UCSC Ensembl
Outerchr15:32169213..32530332hg38UCSC Ensembl
Innerchr15:32471487..32812529hg19UCSC Ensembl
Outerchr15:32461414..32822533hg19UCSC Ensembl
Innerchr15:30258779..30599821hg18UCSC Ensembl
Outerchr15:30248706..30609825hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38361120
hg19361120
hg18361120
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170275
Supporting Variants
SamplesNGO_43
Known GenesCHRNA7, GOLGA8K, GOLGA8O, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247812
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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