A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6587667



Internal ID20960738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69527897..69528632hg38UCSC Ensembl
chr16:69561800..69562535hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244351
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6587667
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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