A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6429864



Internal ID21087417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:108800789..108869706hg38UCSC Ensembl
chr8:109813018..109881935hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3868918
hg1968918
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228549
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6429864
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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