A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522108



Internal ID15449401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:105524175..105535364hg38UCSC Ensembl
Innerchr6:105972050..105983239hg19UCSC Ensembl
Innerchr6:106078743..106089932hg18UCSC Ensembl
Innerchr6:106078743..106089932hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3811190
hg1911190
hg1811190
hg1711190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694880
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522108
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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