A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263939



Internal ID20830979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63903172..63904503hg38UCSC Ensembl
chr3:63888848..63890179hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381332
hg191332
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6547244
Supporting Variants
Samples
Known GenesATXN7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263939
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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