A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467579



Internal ID21125132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33762301..33764600hg38UCSC Ensembl
chr11:33783847..33786146hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382300
hg192300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17990805
Samples
Known GenesFBXO3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467579
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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