A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857919



Internal ID22632854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66389604..66398818hg38UCSC Ensembl
chr15:66681942..66691156hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg389215
hg199215
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473543
Samples
Known GenesMAP2K1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857919
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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