A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6596075



Internal ID20969146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53535476..53536454hg38UCSC Ensembl
chr20:52152015..52152993hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg38979
hg19979
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18253311
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6596075
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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