A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985270



Internal ID21894613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:102270772..102270851hg38UCSC Ensembl
chr2:102887232..102887311hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17528198
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985270
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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