A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv626n223



Internal ID22803594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18547701..18577900hg38UCSC Ensembl
chr10:18836630..18866829hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3830200
hg1930200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6450766, nsv6443747
Samples
Known GenesNSUN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv626n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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