A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526118



Internal ID15453411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:110101478..110132390hg38UCSC Ensembl
Innerchr8:111113707..111144619hg19UCSC Ensembl
Innerchr8:111182883..111213795hg18UCSC Ensembl
Innerchr8:111182883..111213795hg17UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg3830913
hg1930913
hg1830913
hg1730913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv470n21
Supporting Variantsnssv702368
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526118
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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