A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526453



Internal ID15107060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10477556..10480875hg38UCSC Ensembl
Innerchr11:10499103..10502422hg19UCSC Ensembl
Innerchr11:10455679..10458998hg18UCSC Ensembl
Innerchr11:10455679..10458998hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383320
hg193320
hg183320
hg173320
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702756
Samples
Known GenesAMPD3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526453
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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