A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18068862



Internal ID20635902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38768516..38769119hg38UCSC Ensembl
chr20:37397159..37397762hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529670
Supporting Variants
Samples
Known GenesACTR5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18068862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0007


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