A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986387



Internal ID20553427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108880239..108880829hg38UCSC Ensembl
chr11:108750966..108751556hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38591
hg19591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462106
Supporting Variants
Samples
Known GenesDDX10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986387
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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