A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257884



Internal ID20824924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:206007713..206008065hg38UCSC Ensembl
chr2:206872437..206872789hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6537670
Supporting Variants
Samples
Known GenesINO80D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257884
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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