A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519491



Internal ID15100098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:54471593..54734409hg38UCSC Ensembl
Innerchr18:51997963..52401640hg19UCSC Ensembl
Innerchr18:50251961..50552638hg18UCSC Ensembl
Innerchr18:50251961..50552638hg17UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg38262817
hg19403678
hg18300678
hg17300678
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv188n21
Supporting Variantsnssv696880
Samples
Known GenesDYNAP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519491
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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