A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6592508



Internal ID20965579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66980170..66980773hg38UCSC Ensembl
chr16:67014073..67014676hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243589
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6592508
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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