A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908454



Internal ID22683664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63636610..63648679hg38UCSC Ensembl
chr11:63404082..63416151hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3812070
hg1912070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17359325
Samples
Known GenesATL3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908454
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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