A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016822



Internal ID21926165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11086072..11086152hg38UCSC Ensembl
chr10:11128035..11128115hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17590518
Samples
Known GenesCELF2, CELF2-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016822
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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