A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588708



Internal ID20961779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67102239..67102639hg38UCSC Ensembl
chr16:67136142..67136542hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2909n223
Supporting Variantsnssv18243602
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588708
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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