A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6591438



Internal ID20964509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:66413485..66414266hg38UCSC Ensembl
chr16:66447388..66448169hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38782
hg19782
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18243573
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6591438
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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