A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6583729



Internal ID20956800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69169654..69176437hg38UCSC Ensembl
chr16:69203557..69210340hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg386784
hg196784
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244314
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6583729
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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