A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155518



Internal ID22086023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:57130837..57140126hg38UCSC Ensembl
Outerchr18:57129427..57143056hg38UCSC Ensembl
Innerchr18:54798068..54807357hg19UCSC Ensembl
Outerchr18:54796658..54810287hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3813630
hg1913630
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011958
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155518
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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