A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525568



Internal ID15452861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:32144555..32155066hg38UCSC Ensembl
Innerchr19:32635461..32645972hg19UCSC Ensembl
Innerchr19:37327301..37337812hg18UCSC Ensembl
Innerchr19:37327301..37337812hg17UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3810512
hg1910512
hg1810512
hg1710512
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701707
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525568
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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