A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6581311



Internal ID20954382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:80032342..80033191hg38UCSC Ensembl
chr16:80066239..80067088hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg38850
hg19850
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240170
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6581311
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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