A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256001



Internal ID20823041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19602858..19604953hg38UCSC Ensembl
chr2:19802619..19804714hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg382096
hg192096
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6555211
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256001
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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