A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423457



Internal ID21081010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:68869334..68906668hg38UCSC Ensembl
chr8:69781569..69818903hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg3837335
hg1937335
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231655
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423457
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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