A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986144



Internal ID20553184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103386814..103815020hg38UCSC Ensembl
chr11:103257542..103685748hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38428207
hg19428207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6462415
Supporting Variants
Samples
Known GenesDYNC2H1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986144
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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