A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18173091



Internal ID20740131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:89942084..89942422hg38UCSC Ensembl
chr8:90954312..90954650hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431974
Supporting Variants
Samples
Known GenesNBN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18173091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00091


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