A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069110



Internal ID20636150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:58294884..58300177hg38UCSC Ensembl
chr20:56869940..56875233hg19UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg385294
hg195294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6553445
Supporting Variants
Samples
Known GenesPPP4R1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069110
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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