A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv222n209



Internal ID22826297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6551724..6552306hg38UCSC Ensembl
chr11:6572954..6573536hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38583
hg19583
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv5927115, nsv5920243
Samples
Known GenesDNHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)dgv222n209
Frequency
Sample Size914
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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