A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515898



Internal ID15442955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:10672527..10699897hg38UCSC Ensembl
Innerchr8:10530037..10557407hg19UCSC Ensembl
Innerchr8:10567447..10594817hg18UCSC Ensembl
Innerchr8:10567447..10594817hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3827371
hg1927371
hg1827371
hg1727371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv677779, nssv665187
Samples
Known GenesC8orf74
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515898
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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