A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6594421



Internal ID20967492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69092620..69093565hg38UCSC Ensembl
chr16:69126523..69127468hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38946
hg19946
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18244308
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6594421
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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