A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528826



Internal ID15109433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46077896..46120751hg38UCSC Ensembl
Innerchr19:46581154..46624008hg19UCSC Ensembl
Innerchr19:51272994..51315848hg18UCSC Ensembl
Innerchr19:51272994..51315848hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3842856
hg1942855
hg1842855
hg1742855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705500
Samples
Known GenesIGFL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528826
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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