A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831712



Internal ID22606647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:162021337..162034654hg38UCSC Ensembl
chr2:162877847..162891164hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3813318
hg1913318
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480616
Samples
Known GenesDPP4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5831712
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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