A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519912



Internal ID15447205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:26475207..26491362hg38UCSC Ensembl
Innerchr8:26332723..26348878hg19UCSC Ensembl
Innerchr8:26388640..26404795hg18UCSC Ensembl
Innerchr8:26388640..26404795hg17UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3816156
hg1916156
hg1816156
hg1716156
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697120
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519912
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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