A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434038



Internal ID21091591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66554126..66579434hg38UCSC Ensembl
chr8:67466361..67491669hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg3825309
hg1925309
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223502
Samples
Known GenesMYBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434038
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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