A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985565



Internal ID21894908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113130585..113130761hg38UCSC Ensembl
chr2:113888162..113888338hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531401
Samples
Known GenesIL1RN
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985565
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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