A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858856



Internal ID22633791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92970059..92974533hg38UCSC Ensembl
chr11:92703225..92707699hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg384475
hg194475
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458028
Samples
Known GenesMTNR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858856
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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