A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538982



Internal ID20912289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32956042..32957477hg38UCSC Ensembl
chr3:32997534..32998969hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg381436
hg191436
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262023
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538982
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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