A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6593906



Internal ID20966977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68135730..68136436hg38UCSC Ensembl
chr16:68169633..68170339hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38707
hg19707
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243638
Samples
Known GenesNFATC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6593906
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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