A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032293



Internal ID19121515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119298868..119377333hg38UCSC Ensembl
Innerchr8:120311108..120389573hg19UCSC Ensembl
Innerchr8:120380289..120458754hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3878466
hg1978466
hg1878466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691467
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)nsv1032293
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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