A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925154



Internal ID22700381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:132744927..132744981hg38UCSC Ensembl
chr11:132614822..132614876hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17353982
Samples
Known GenesOPCML
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925154
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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