A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18092928



Internal ID20659968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104358701..104551500hg38UCSC Ensembl
chr3:104077545..104270344hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg38192800
hg19192800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368651
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18092928
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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