A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18208366



Internal ID20775406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237890456..237925443hg38UCSC Ensembl
chr2:238799098..238834085hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3834988
hg1934988
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6337133
Supporting Variants
Samples
Known GenesRAMP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18208366
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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