A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419175



Internal ID21076728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:110519657..110847552hg38UCSC Ensembl
chr8:111531886..111859781hg19UCSC Ensembl
Cytoband8q23.2
Allele length
AssemblyAllele length
hg38327896
hg19327896
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227849
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419175
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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