A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6543876



Internal ID20917117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:54912223..54918355hg38UCSC Ensembl
chr20:53528762..53534894hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg386133
hg196133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18070223
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6543876
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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