A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18225053



Internal ID20792093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:136935301..137021100hg38UCSC Ensembl
chr8:137947544..138033343hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3885800
hg1985800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6430650
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18225053
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.0001


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