A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166576



Internal ID20733616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139719100..139719734hg38UCSC Ensembl
chr8:140731343..140731977hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425196
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166576
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00044


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