A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6555428



Internal ID20928515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:16488409..16489327hg38UCSC Ensembl
chr3:16529916..16530834hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38919
hg19919
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18261109
Samples
Known GenesRFTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6555428
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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