A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015515



Internal ID19104732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:114143109..114198049hg38UCSC Ensembl
Innerchr8:115155338..115210278hg19UCSC Ensembl
Innerchr8:115224514..115279454hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3854941
hg1954941
hg1854941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7288n100
Supporting Variantsnssv3691318
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)nsv1015515
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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