A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206013



Internal ID20773053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25716835..25730416hg38UCSC Ensembl
chr21:27089147..27102727hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3813582
hg1913581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537024
Supporting Variants
Samples
Known GenesATP5J, JAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206013
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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