A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915183



Internal ID22690401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:47165625..47165779hg38UCSC Ensembl
chr11:47187176..47187330hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356501
Samples
Known GenesARFGAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915183
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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