A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5908296



Internal ID22683506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5476751..5477270hg38UCSC Ensembl
chr11:5497981..5498500hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365081
Samples
Known GenesOR51B5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5908296
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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