A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6564181



Internal ID20937252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189224446..189225108hg38UCSC Ensembl
chr3:188942235..188942897hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261880
Samples
Known GenesTPRG1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6564181
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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