A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067856



Internal ID20634896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53256601..53261100hg38UCSC Ensembl
chr20:51873140..51877639hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6541620
Supporting Variants
Samples
Known GenesTSHZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067856
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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