A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256974



Internal ID20824014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:189979156..189992677hg38UCSC Ensembl
chr2:190843882..190857403hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg3813522
hg1913522
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6552838
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256974
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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