A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161392



Internal ID20728432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101375301..101391600hg38UCSC Ensembl
chr8:102387529..102403828hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg3816300
hg1916300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418412
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00148


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