A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543065



Internal ID20916316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48116493..48117410hg38UCSC Ensembl
chr3:48157983..48158900hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38918
hg19918
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262128
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543065
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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