A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18169414



Internal ID20736454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:66565976..66566497hg38UCSC Ensembl
chr8:67478211..67478732hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427632
Supporting Variants
Samples
Known GenesMYBL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18169414
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00035


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