A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6538698



Internal ID20912012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42788602..42789339hg38UCSC Ensembl
chr3:42830094..42830831hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38738
hg19738
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18260687
Samples
Known GenesHIGD1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6538698
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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