A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6565923



Internal ID20938994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:129755906..129756475hg38UCSC Ensembl
chr3:129474749..129475318hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38570
hg19570
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18259631
Samples
Known GenesTMCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6565923
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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