A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020268



Internal ID19109487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:101267093..101300013hg38UCSC Ensembl
Innerchr8:102279321..102312241hg19UCSC Ensembl
Innerchr8:102348497..102381417hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3832921
hg1932921
hg1832921
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689747
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020268
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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