A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6549285



Internal ID20922453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:82885471..82886715hg38UCSC Ensembl
chr3:82934622..82935866hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg381245
hg191245
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262364
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6549285
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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