A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879879



Internal ID22654849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4105563..4107462hg38UCSC Ensembl
chr19:4105561..4107460hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17475951
Samples
Known GenesMAP2K2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879879
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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