A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18106707



Internal ID20673747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:94349788..94350943hg38UCSC Ensembl
chr3:94068632..94069787hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg381156
hg191156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362097
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18106707
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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