A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899630



Internal ID22674761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109106809..109107674hg38UCSC Ensembl
chr6:109428012..109428877hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38866
hg19866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17414320
Samples
Known GenesCEP57L1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5899630
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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