A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18255309



Internal ID20822349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:157343317..157345330hg38UCSC Ensembl
chr2:158199829..158201842hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg382014
hg192014
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6550389
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18255309
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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