A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991059



Internal ID20558099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40112382..40112820hg38UCSC Ensembl
chr11:40133932..40134370hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38439
hg19439
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460930
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991059
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00136


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