A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561958



Internal ID334924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92970799..92971204hg38UCSC Ensembl
chr11:92703965..92704370hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052023
Samples
Known GenesMTNR1B
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561958
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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