A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921371



Internal ID22696594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108209329..108217463hg38UCSC Ensembl
chr11:108080056..108088190hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg388135
hg198135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351423
Samples
Known GenesNPAT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921371
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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