A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527414



Internal ID15454707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:110206628..110449907hg38UCSC Ensembl
Innerchr8:111218857..111462136hg19UCSC Ensembl
Innerchr8:111288033..111531312hg18UCSC Ensembl
Innerchr8:111288033..111531312hg17UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg38243280
hg19243280
hg18243280
hg17243280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703852
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527414
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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