A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5917079



Internal ID22692298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:128214728..128214806hg38UCSC Ensembl
chr11:128084623..128084701hg19UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5917079
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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