A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5987199



Internal ID21896542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:189343985..189408366hg38UCSC Ensembl
chr2:190208711..190273092hg19UCSC Ensembl
Cytoband2q32.2
Allele length
AssemblyAllele length
hg3864382
hg1964382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17524364
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5987199
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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