A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977741



Internal ID22752676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28117260..28117260hg38UCSC Ensembl
chr11:28138807..28138807hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17362871
Samples
Known GenesMETTL15
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977741
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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