A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418974



Internal ID21076527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:58671833..58687524hg38UCSC Ensembl
chr8:59584392..59600083hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg3815692
hg1915692
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223700
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418974
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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