A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6573192



Internal ID20946263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:139463832..139464268hg38UCSC Ensembl
chr6:139784969..139785405hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18272501
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6573192
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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