A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18099166



Internal ID20666206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:4071482..4101925hg38UCSC Ensembl
chr3:4113166..4143609hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3830444
hg1930444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374564
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18099166
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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