A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032636



Internal ID19121858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83565678..83608312hg38UCSC Ensembl
Innerchr8:84477913..84520547hg19UCSC Ensembl
Innerchr8:84640468..84683102hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3842635
hg1942635
hg1842635
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7248n100
Supporting Variantsnssv3689601
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)nsv1032636
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