A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914201



Internal ID22689418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71261007..71264017hg38UCSC Ensembl
chr11:70972053..70975063hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg383011
hg193011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17361210
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914201
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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