A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594330



Internal ID20967401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4759637..4763320hg38UCSC Ensembl
chr16:4809638..4813321hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg383684
hg193684
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240660
Samples
Known GenesZNF500
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594330
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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