A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422737



Internal ID21080290
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:106870472..106897328hg38UCSC Ensembl
chr8:107882700..107909556hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg3826857
hg1926857
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220503
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422737
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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