A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985389



Internal ID21894732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102003002..102003186hg38UCSC Ensembl
chr2:102619464..102619648hg19UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520337
Samples
Known GenesIL1R2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985389
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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