A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525186



Internal ID15452479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45493390..45495909hg38UCSC Ensembl
Innerchr20:44122030..44124549hg19UCSC Ensembl
Innerchr20:43555444..43557963hg18UCSC Ensembl
Innerchr20:43555444..43557963hg17UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg382520
hg192520
hg182520
hg172520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701264
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525186
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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