A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992863



Internal ID20559903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71280509..71283030hg38UCSC Ensembl
chr11:70991555..70994076hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg382522
hg192522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6467384
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992863
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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