A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097590



Internal ID20664630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184204816..184217550hg38UCSC Ensembl
chr3:183922604..183935338hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3812735
hg1912735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362215
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097590
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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