A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261457



Internal ID20828497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:54275639..54276288hg38UCSC Ensembl
chr3:54309666..54310315hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540955
Supporting Variants
Samples
Known GenesCACNA2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261457
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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