A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993799



Internal ID20560839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63600114..63605052hg38UCSC Ensembl
chr11:63367586..63372524hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg384939
hg194939
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463120
Supporting Variants
Samples
Known GenesPLA2G16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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