A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914774



Internal ID22689991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66090951..66091264hg38UCSC Ensembl
chr11:65858422..65858735hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38314
hg19314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17352151
Samples
Known GenesPACS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914774
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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