A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6558089



Internal ID20931160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:152934471..152935485hg38UCSC Ensembl
chr3:152652260..152653274hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg381015
hg191015
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18263240
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6558089
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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