A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18166560



Internal ID20733600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:139507255..139517644hg38UCSC Ensembl
chr8:140519498..140529887hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3810390
hg1910390
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6435358
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18166560
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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