A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914569



Internal ID22689786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34443162..34444651hg38UCSC Ensembl
chr11:34464709..34466198hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg381490
hg191490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354064
Samples
Known GenesCAT
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914569
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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