A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032321



Internal ID19121543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:62041505..62114008hg38UCSC Ensembl
Innerchr8:62954064..63026567hg19UCSC Ensembl
Innerchr8:63116618..63189121hg18UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg3872504
hg1972504
hg1872504
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689472
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)nsv1032321
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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