A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495232



Internal ID272351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10805663..10805747hg38UCSC Ensembl
chr11:10827210..10827294hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043298
Samples
Known GenesEIF4G2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495232
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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