A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17989496



Internal ID20556536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:21979284..22005319hg38UCSC Ensembl
chr11:22000830..22026865hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3826036
hg1926036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454036
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17989496
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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