A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18067880



Internal ID20634920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53669018..53675350hg38UCSC Ensembl
chr20:52285557..52291889hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg386333
hg196333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6548334
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18067880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.01838


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