A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18256268



Internal ID20823308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:168549504..168550415hg38UCSC Ensembl
chr2:169406014..169406925hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg38912
hg19912
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547540
Supporting Variants
Samples
Known GenesCERS6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18256268
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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