A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6568242



Internal ID20941313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189335462..189335593hg38UCSC Ensembl
chr3:189053251..189053382hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261883
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6568242
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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