A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851402



Internal ID22626337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:78796084..78804262hg38UCSC Ensembl
chr11:78507129..78515307hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg388179
hg198179
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455064
Samples
Known GenesTENM4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851402
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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