A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6540955



Internal ID20914242
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 StatusM
Merged Variants
Supporting Variantsnssv18261457
Samples
Known GenesCACNA2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6540955
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer