A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993826



Internal ID20560866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63975507..63975799hg38UCSC Ensembl
chr11:63742979..63743271hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474041
Supporting Variants
Samples
Known GenesCOX8A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993826
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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