A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590283



Internal ID20963354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66858110..66858592hg38UCSC Ensembl
chr16:66892013..66892495hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243587
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590283
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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