A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235873



Internal ID20802913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:137721805..137740522hg38UCSC Ensembl
chr8:138734048..138752765hg19UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg3818718
hg1918718
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6416764
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235873
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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