A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027718



Internal ID18770250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:22805950..23258334hg38UCSC Ensembl
Innerchr8:22663463..23115847hg19UCSC Ensembl
Innerchr8:22719408..23171792hg18UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg38452385
hg19452385
hg18452385
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3685369
Samples
Known GenesCHMP7, LOC254896, LOC286059, LOC389641, PEBP4, RHOBTB2, TNFRSF10A, TNFRSF10B, TNFRSF10C, TNFRSF10D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027718
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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