A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593122



Internal ID20966193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63650454..63651180hg38UCSC Ensembl
chr16:63684358..63685084hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38727
hg19727
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240059
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593122
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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