A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155517



Internal ID22086022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:53658829..53670518hg38UCSC Ensembl
Outerchr18:53657908..53672408hg38UCSC Ensembl
Innerchr18:51185199..51196888hg19UCSC Ensembl
Outerchr18:51184278..51198778hg19UCSC Ensembl
Cytoband18q21.2
Allele length
AssemblyAllele length
hg3814501
hg1914501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011957
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155517
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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