A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18209108



Internal ID20776148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:24999695..25016672hg38UCSC Ensembl
chr2:25222564..25239541hg19UCSC Ensembl
Cytoband2p23.3
Allele length
AssemblyAllele length
hg3816978
hg1916978
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6351240
Supporting Variants
Samples
Known GenesDNAJC27-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18209108
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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