A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020115



Internal ID18762651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:86099478..86155561hg38UCSC Ensembl
Innerchr8:87111707..87167790hg19UCSC Ensembl
Innerchr8:87180823..87236906hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3856084
hg1956084
hg1856084
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7262n100
Supporting Variantsnssv3689672
Samples
Known GenesATP6V0D2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020115
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer