A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173078



Internal ID20740118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89823982..89846735hg38UCSC Ensembl
chr8:90836210..90858963hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3822754
hg1922754
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422024
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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