A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099892



Internal ID20666932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4224484..4265171hg38UCSC Ensembl
chr3:4266168..4306855hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3840688
hg1940688
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375114
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099892
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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