A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18069185



Internal ID20636225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:59940389..59940461hg38UCSC Ensembl
chr20:58515444..58515516hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6549232
Supporting Variants
Samples
Known GenesFAM217B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18069185
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02343


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