A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596153



Internal ID20969224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53887317..53925162hg38UCSC Ensembl
chr20:52503856..52541701hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3837846
hg1937846
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253349
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596153
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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