A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5969966



Internal ID22744901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101041048..101041048hg38UCSC Ensembl
chr11:100911779..100911779hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358103
Samples
Known GenesPGR
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5969966
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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