A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18095096



Internal ID20662136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:162305701..162359100hg38UCSC Ensembl
chr3:162023489..162076888hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3853400
hg1953400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374059
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18095096
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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