A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105267



Internal ID20672307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78280253..78281214hg38UCSC Ensembl
chr3:78329403..78330364hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38962
hg19962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363769
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105267
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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