A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914506



Internal ID22689723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9250862..9252376hg38UCSC Ensembl
chr11:9272409..9273923hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381515
hg191515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365799
Samples
Known GenesDENND5A
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914506
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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