A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17363676



Internal ID22589345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93793114..93793114hg38UCSC Ensembl
chr11:93526280..93526280hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971422
Supporting Variants
Samples
Known GenesMED17
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17363676
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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