A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178904



Internal ID20745944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:86052517..86072624hg38UCSC Ensembl
chr11:85763559..85783666hg19UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3820108
hg1920108
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462899
Supporting Variants
Samples
Known GenesPICALM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178904
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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