A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5924170



Internal ID22699397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:116807279..116816825hg38UCSC Ensembl
chr11:116677995..116687541hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg389547
hg199547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5924170
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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