A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18093220



Internal ID20660260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129368357..129371744hg38UCSC Ensembl
chr3:129087200..129090587hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg383388
hg193388
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6374764
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18093220
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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