A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155501



Internal ID22086006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:8789079..8836199hg38UCSC Ensembl
Outerchr18:8787859..8836490hg38UCSC Ensembl
Innerchr18:8789077..8836197hg19UCSC Ensembl
Outerchr18:8787857..8836488hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3848632
hg1948632
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011883
Samples
Known GenesSOGA2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155501
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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