A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993814



Internal ID20560854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63786201..63791400hg38UCSC Ensembl
chr11:63553673..63558872hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg385200
hg195200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6470882
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993814
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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