A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205613



Internal ID20772653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:159776090..159776841hg38UCSC Ensembl
chr2:160632601..160633352hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38752
hg19752
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6341867
Supporting Variants
Samples
Known GenesCD302, LY75-CD302
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205613
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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