A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986026



Internal ID20553066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103698295..103709612hg38UCSC Ensembl
chr11:103569023..103580340hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3811318
hg1911318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463381
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986026
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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