A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167919



Internal ID20734959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25879832..25880261hg38UCSC Ensembl
chr8:25737348..25737777hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38430
hg19430
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426329
Supporting Variants
Samples
Known GenesEBF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167919
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00012


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