A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016529



Internal ID19105748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114134599..114198049hg38UCSC Ensembl
Innerchr8:115146828..115210278hg19UCSC Ensembl
Innerchr8:115216004..115279454hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3863451
hg1963451
hg1863451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7288n100
Supporting Variantsnssv3691317, nssv3691316
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)nsv1016529
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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