A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591824



Internal ID20964895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68195526..68196225hg38UCSC Ensembl
chr16:68229429..68230128hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243642
Samples
Known GenesNFATC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591824
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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