A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985374



Internal ID21894717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11104246..11104348hg38UCSC Ensembl
chr2:11244372..11244474hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536120
Samples
Known GenesFLJ33534
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985374
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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