A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6588898



Internal ID20961969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:34588347..34956072hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38367726
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2835n223
Supporting Variantsnssv18239984
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6588898
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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