A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018781



Internal ID19107998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:121391755..121426457hg38UCSC Ensembl
Innerchr8:122403995..122438697hg19UCSC Ensembl
Innerchr8:122473176..122507878hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3834703
hg1934703
hg1834703
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7303n100
Supporting Variantsnssv3691482
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)nsv1018781
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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