A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420179



Internal ID21077732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:92426001..92433200hg38UCSC Ensembl
chr8:93438229..93445428hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg387200
hg197200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236853
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420179
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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