A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180577



Internal ID20747617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65022740..65024112hg38UCSC Ensembl
chr11:64790212..64791584hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381373
hg191373
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6468196
Supporting Variants
Samples
Known GenesARL2-SNX15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180577
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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