A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263940



Internal ID20830980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63922057..63923793hg38UCSC Ensembl
chr3:63907733..63909469hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381737
hg191737
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553158
Supporting Variants
Samples
Known GenesATXN7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263940
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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