A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018024



Internal ID19107241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:90737088..90774759hg38UCSC Ensembl
Innerchr8:91749316..91786987hg19UCSC Ensembl
Innerchr8:91818492..91856163hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3837672
hg1937672
hg1837672
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7267n100
Supporting Variantsnssv3689710
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)nsv1018024
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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