A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178221



Internal ID20745261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:105060301..105266410hg38UCSC Ensembl
chr11:104931028..105137137hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38206110
hg19206110
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456078
Supporting Variants
Samples
Known GenesCARD17, CARD18
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178221
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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