A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456138



Internal ID21113691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92971204..92974845hg38UCSC Ensembl
chr11:92704370..92708011hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg383642
hg193642
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18191769
Samples
Known GenesMTNR1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456138
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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