A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418616



Internal ID21076169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:116775813..116837750hg38UCSC Ensembl
chr8:117788052..117849989hg19UCSC Ensembl
Cytoband8q24.11
Allele length
AssemblyAllele length
hg3861938
hg1961938
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228217
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418616
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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