A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210687



Internal ID20777727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:91436001..91522600hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3886600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6343938
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210687
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.46177


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