A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101851



Internal ID20668891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26781204..26791622hg38UCSC Ensembl
chr3:26822695..26833113hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3810419
hg1910419
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360852
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101851
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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