A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558795



Internal ID20931866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189610656..189612389hg38UCSC Ensembl
chr3:189328445..189330178hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg381734
hg191734
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5127n223
Supporting Variantsnssv18261885
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558795
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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