A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6445363



Internal ID21102916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92197932..92222636hg38UCSC Ensembl
chr10:93957689..93982393hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg3824705
hg1924705
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985398
Samples
Known GenesCPEB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6445363
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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