A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596105



Internal ID20969176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:6406881..6423196hg38UCSC Ensembl
chr20:6387528..6403843hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3816316
hg1916316
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18254098
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596105
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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