A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597806



Internal ID20970877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:5587442..5588522hg38UCSC Ensembl
chr20:5568088..5569168hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253386
Samples
Known GenesGPCPD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6597806
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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