A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517996



Internal ID15445289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:77619641..77706340hg38UCSC Ensembl
Innerchr18:75331597..75418296hg19UCSC Ensembl
Innerchr18:73460585..73547284hg18UCSC Ensembl
Innerchr18:73460585..73547284hg17UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3886700
hg1986700
hg1886700
hg1786700
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695408
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517996
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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