A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169022



Internal ID20736062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39288192..39288624hg38UCSC Ensembl
chr8:39145711..39146143hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425341
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169022
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00026


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