A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18172890



Internal ID20739930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92693801..92696400hg38UCSC Ensembl
chr8:93706029..93708628hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425763
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18172890
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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