A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099401



Internal ID20666441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32546563..32548100hg38UCSC Ensembl
chr3:32588055..32589592hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381538
hg191538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361882
Supporting Variants
Samples
Known GenesDYNC1LI1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099401
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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