A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528566



Internal ID15455859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:104402228..104484775hg38UCSC Ensembl
Innerchr1:104944850..105027397hg19UCSC Ensembl
Innerchr1:104746373..104828920hg18UCSC Ensembl
Innerchr1:104656871..104739418hg17UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3882548
hg1982548
hg1882548
hg1782548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705185
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528566
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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