A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5900028



Internal ID22675166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:162051132..162052968hg38UCSC Ensembl
chr2:162907642..162909478hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg381837
hg191837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17404937
Samples
Known GenesDPP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5900028
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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