A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18260029



Internal ID20827069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:39313657..39314441hg38UCSC Ensembl
chr3:39355148..39355932hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg38785
hg19785
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553779
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18260029
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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