A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223102



Internal ID20790142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96028884..96029316hg38UCSC Ensembl
chr13:96681138..96681570hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6592280
Supporting Variants
Samples
Known GenesUGGT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223102
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00014


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