A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433826



Internal ID21091379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:93840711..93873540hg38UCSC Ensembl
chr8:94852939..94885768hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3832830
hg1932830
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230573
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433826
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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