A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5987234



Internal ID21896577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:195568358..195568534hg38UCSC Ensembl
chr2:196433082..196433258hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17518008
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv5987234
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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