A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027259



Internal ID19116478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:116778689..116829816hg38UCSC Ensembl
Innerchr8:117790928..117842055hg19UCSC Ensembl
Innerchr8:117860109..117911236hg18UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg3851128
hg1951128
hg1851128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7301n100
Supporting Variantsnssv3691461
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)nsv1027259
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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