A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016449



Internal ID19105668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:116618444..116631906hg38UCSC Ensembl
Innerchr8:117630683..117644145hg19UCSC Ensembl
Innerchr8:117699864..117713326hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3813463
hg1913463
hg1813463
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7300n100
Supporting Variantsnssv3691458
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)nsv1016449
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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