A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17987035



Internal ID20554076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121807922..121832530hg38UCSC Ensembl
chr11:121678630..121703238hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg3824609
hg1924609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6466185
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17987035
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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