A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6590640



Internal ID20963711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:54031029..54032416hg38UCSC Ensembl
chr16:54064941..54066328hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg381388
hg191388
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240727
Samples
Known GenesFTO
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6590640
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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