A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523986



Internal ID15451279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4781898..4784541hg38UCSC Ensembl
Innerchr19:4781910..4784553hg19UCSC Ensembl
Innerchr19:4732910..4735553hg18UCSC Ensembl
Innerchr19:4732910..4735553hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg382644
hg192644
hg182644
hg172644
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699842
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523986
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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