A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522228



Internal ID15449521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:78901677..78916102hg38UCSC Ensembl
Innerchr18:76661677..76676102hg19UCSC Ensembl
Innerchr18:74762665..74777090hg18UCSC Ensembl
Innerchr18:74762665..74777090hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3814426
hg1914426
hg1814426
hg1714426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695005
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522228
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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