A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553091



Internal ID20926206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:54982919..54984699hg38UCSC Ensembl
chr3:55016946..55018726hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg381781
hg191781
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261466
Samples
Known GenesCACNA2D3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553091
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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