A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6572962



Internal ID20946033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182951424..182951851hg38UCSC Ensembl
chr3:182669212..182669639hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38428
hg19428
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261835
Samples
Known GenesDCUN1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6572962
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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