A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588597



Internal ID20961668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68128922..68129604hg38UCSC Ensembl
chr16:68162825..68163507hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38683
hg19683
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243637
Samples
Known GenesNFATC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588597
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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