A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105164



Internal ID20672205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77316774..77317362hg38UCSC Ensembl
chr3:77365925..77366513hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38589
hg19589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6364381
Supporting Variants
Samples
Known GenesROBO2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105164
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00024


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