A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17992701



Internal ID20559741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69299568..69304963hg38UCSC Ensembl
chr11:69067035..69072430hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg385396
hg195396
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6474464
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17992701
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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