A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993939



Internal ID20560979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82023001..82025400hg38UCSC Ensembl
chr11:81734043..81736442hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464656
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993939
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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