A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097598



Internal ID20664638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184393567..184395717hg38UCSC Ensembl
chr3:184111355..184113505hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg382151
hg192151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372975
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097598
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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