A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519453



Internal ID15446746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29375578..29384096hg38UCSC Ensembl
Innerchr6:29343355..29351873hg19UCSC Ensembl
Innerchr6:29451334..29459852hg18UCSC Ensembl
Innerchr6:29451334..29459852hg17UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg388519
hg198519
hg188519
hg178519
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702300, nssv656239, nssv686457, nssv703903, nssv695882
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519453
Frequency
Sample Size2026
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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