A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020359



Internal ID18762894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102097693..102306187hg38UCSC Ensembl
Innerchr8:103109921..103318415hg19UCSC Ensembl
Innerchr8:103179097..103387591hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38208495
hg19208495
hg18208495
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691254
Samples
Known GenesMIR5680, NCALD, RRM2B, UBR5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020359
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