A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520947



Internal ID15448240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:51974981..52003434hg38UCSC Ensembl
Innerchr8:52887541..52915994hg19UCSC Ensembl
Innerchr8:53050094..53078547hg18UCSC Ensembl
Innerchr8:53050094..53078547hg17UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3828454
hg1928454
hg1828454
hg1728454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697703
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520947
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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