A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18261456



Internal ID20828496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:54245564..54499063hg38UCSC Ensembl
chr3:54279591..54533090hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg38253500
hg19253500
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6538027
Supporting Variants
Samples
Known GenesCACNA2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18261456
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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