A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212322



Internal ID20779362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:60402502..60663724hg38UCSC Ensembl
chr3:60388235..60649457hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38261223
hg19261223
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362213
Supporting Variants
Samples
Known GenesFHIT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212322
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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