A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416618



Internal ID21074171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66491193..66492725hg38UCSC Ensembl
chr8:67403428..67404960hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg381533
hg191533
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228344
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416618
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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