A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18223502



Internal ID20790542
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 StatusS
Merged Variantsnsv6434038
Supporting Variants
Samples
Known GenesMYBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18223502
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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