A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6578870



Internal ID20951941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:53862194..53862511hg38UCSC Ensembl
chr16:53896106..53896423hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240725
Samples
Known GenesFTO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6578870
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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