A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033691



Internal ID19122912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:83860934..83897254hg38UCSC Ensembl
Innerchr8:84773169..84809489hg19UCSC Ensembl
Innerchr8:84935724..84972044hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3836321
hg1936321
hg1836321
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7250n100
Supporting Variantsnssv3757303
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)nsv1033691
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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