A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6584126



Internal ID20957197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69622960..69623745hg38UCSC Ensembl
chr16:69656863..69657648hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38786
hg19786
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244364
Samples
Known GenesNFAT5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6584126
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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