A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169639



Internal ID20736679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:71653725..71676043hg38UCSC Ensembl
chr8:72565960..72588278hg19UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3822319
hg1922319
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416343
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169639
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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