A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18165699



Internal ID20732739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:132551752..132552092hg38UCSC Ensembl
chr8:133563999..133564339hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6423843
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18165699
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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