A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173075



Internal ID20740115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89795601..89797900hg38UCSC Ensembl
chr8:90807829..90810128hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423536
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173075
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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