A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18168366



Internal ID20735406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:53187486..53188118hg38UCSC Ensembl
chr8:54100046..54100678hg19UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg38633
hg19633
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426915
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18168366
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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