A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209906



Internal ID20776946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:53557944..53615271hg38UCSC Ensembl
chr2:53785081..53842408hg19UCSC Ensembl
Cytoband2p16.2
Allele length
AssemblyAllele length
hg3857328
hg1957328
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354553
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209906
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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