A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161394



Internal ID20728434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:101395112..101397427hg38UCSC Ensembl
chr8:102407340..102409655hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg382316
hg192316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432744
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161394
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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