A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5927281



Internal ID22702509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:107465320..107477470hg38UCSC Ensembl
chr11:107336046..107348196hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3812151
hg1912151
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350624
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5927281
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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