A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986409



Internal ID20553449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:109088892..109168466hg38UCSC Ensembl
chr11:108959619..109039193hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3879575
hg1979575
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456211
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986409
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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