A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435452



Internal ID21093005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:126817846..126858964hg38UCSC Ensembl
chr8:127830091..127871209hg19UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3841119
hg1941119
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236931
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435452
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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