A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848125



Internal ID22623060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66950232..66963397hg38UCSC Ensembl
chr11:66717703..66730868hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3813166
hg1913166
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460141
Samples
Known GenesPC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848125
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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