A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18271089



Internal ID20838129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:121169711..121180077hg38UCSC Ensembl
chr6:121490857..121501223hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3810367
hg1910367
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6564047
Supporting Variants
Samples
Known GenesTBC1D32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18271089
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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