A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995893



Internal ID20562933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:98141348..98425816hg38UCSC Ensembl
chr11:98012076..98296545hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38284469
hg19284470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460539
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995893
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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