A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426043



Internal ID21083596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:74768401..74773800hg38UCSC Ensembl
chr8:75680636..75686035hg19UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223371
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426043
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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