A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18163981



Internal ID20731021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:122587604..122591446hg38UCSC Ensembl
chr8:123599843..123603685hg19UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg383843
hg193843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427213
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18163981
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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