A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909105



Internal ID22684315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18584644..18600213hg38UCSC Ensembl
chr11:18606191..18621760hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3815570
hg1915570
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353884
Samples
Known GenesSPTY2D1-AS1, UEVLD
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909105
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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