A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205606



Internal ID20772646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:159161338..159326653hg38UCSC Ensembl
chr2:160017849..160183164hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38165316
hg19165316
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6350173
Supporting Variants
Samples
Known GenesBAZ2B, MIR6888, TANC1, WDSUB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205606
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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