A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986043



Internal ID20553083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:103934617..103935137hg38UCSC Ensembl
chr11:103805345..103805865hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38521
hg19521
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6458028
Supporting Variants
Samples
Known GenesPDGFD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986043
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00055


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