A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522565



Internal ID15449858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29395627..29403898hg38UCSC Ensembl
Innerchr19:29886534..29894805hg19UCSC Ensembl
Innerchr19:34578374..34586645hg18UCSC Ensembl
Innerchr19:34578374..34586645hg17UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg388272
hg198272
hg188272
hg178272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705948
Samples
Known GenesLOC284395
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522565
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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