A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv903n223



Internal ID22803871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121008901..121029100hg38UCSC Ensembl
chr10:122768414..122788613hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3820200
hg1920200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6439273, nsv6444826, nsv6436338
Samples
Known GenesMIR5694
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv903n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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