A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5985988



Internal ID21895331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:128448047..128448119hg38UCSC Ensembl
chr2:129205621..129205693hg19UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17525870
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5985988
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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