A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424523



Internal ID21082076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:104631401..104635100hg38UCSC Ensembl
chr8:105643629..105647328hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg383700
hg193700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223299
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424523
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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