A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208999



Internal ID20776039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:240629411..240634676hg38UCSC Ensembl
chr2:241568828..241574093hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg385266
hg195266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6354332
Supporting Variants
Samples
Known GenesGPR35
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208999
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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