A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260154



Internal ID20827194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:35564834..35749554hg38UCSC Ensembl
chr2:35789900..35974620hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38184721
hg19184721
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540119
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260154
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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