A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528067



Internal ID15455360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:48856895..48867388hg38UCSC Ensembl
Innerchr8:49769454..49779947hg19UCSC Ensembl
Innerchr8:49932007..49942500hg18UCSC Ensembl
Innerchr8:49932007..49942500hg17UCSC Ensembl
Cytoband8q11.21
Allele length
AssemblyAllele length
hg3810494
hg1910494
hg1810494
hg1710494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704603
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528067
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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