A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6595956



Internal ID20969027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:1143815..1145178hg38UCSC Ensembl
chr20:1124458..1125821hg19UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg381364
hg191364
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253474
Samples
Known GenesPSMF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6595956
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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