A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102134



Internal ID20669174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37186139..37189791hg38UCSC Ensembl
chr3:37227630..37231282hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg383653
hg193653
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362649
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102134
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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