A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178590



Internal ID20745630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:104027401..104053600hg38UCSC Ensembl
chr11:103898129..103924328hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3826200
hg1926200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6461712
Supporting Variants
Samples
Known GenesDDI1, PDGFD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178590
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00036


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