A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023965



Internal ID19113182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85492906..85539935hg38UCSC Ensembl
Innerchr8:86405135..86452164hg19UCSC Ensembl
Innerchr8:86592387..86639416hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3847030
hg1947030
hg1847030
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689646
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)nsv1023965
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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