A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596903



Internal ID20969974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53556329..53557896hg38UCSC Ensembl
chr20:52172868..52174435hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg381568
hg191568
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253316
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596903
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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