A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6553779



Internal ID20926892
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 StatusM
Merged Variantsdgv4848n223
Supporting Variantsnssv18260029
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6553779
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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