A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18167910



Internal ID20734950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:25754080..25787957hg38UCSC Ensembl
chr8:25611596..25645473hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg3833878
hg1933878
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423334
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18167910
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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