A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6554982



Internal ID20928071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:24350251..24366214hg38UCSC Ensembl
chr3:24391742..24407705hg19UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3815964
hg1915964
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18262597
Samples
Known GenesTHRB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6554982
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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