A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993798



Internal ID20560838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63596016..63597299hg38UCSC Ensembl
chr11:63363488..63364771hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381284
hg191284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467673
Supporting Variants
Samples
Known GenesPLA2G16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993798
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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