A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5989257



Internal ID21898600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:38756187..38756306hg38UCSC Ensembl
chr2:38983329..38983448hg19UCSC Ensembl
Cytoband2p22.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531809
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5989257
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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