A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205614



Internal ID20772654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:159845703..160009146hg38UCSC Ensembl
chr2:160702214..160865657hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38163444
hg19163444
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6353702
Supporting Variants
Samples
Known GenesLY75, LY75-CD302, PLA2R1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205614
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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