A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6598190



Internal ID20971261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53096346..53096830hg38UCSC Ensembl
chr20:51712885..51713369hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253301
Samples
Known GenesTSHZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6598190
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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