A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18257324



Internal ID20824364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231334682..231337047hg38UCSC Ensembl
chr2:232199394..232201759hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg382366
hg192366
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6546886
Supporting Variants
Samples
Known GenesARMC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18257324
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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