A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993454



Internal ID20560494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63067201..63076800hg38UCSC Ensembl
chr11:62834673..62844272hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg389600
hg199600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456709
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993454
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00543


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