A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17991135



Internal ID20558175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47198457..47200825hg38UCSC Ensembl
chr11:47220008..47222376hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg382369
hg192369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474674
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17991135
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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