A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18273329



Internal ID20840369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63546543..63547345hg38UCSC Ensembl
chr6:64256448..64257250hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38803
hg19803
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6556390
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18273329
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00015


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