A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5512148



Internal ID288714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32600832..32601710hg38UCSC Ensembl
chr11:32622378..32623256hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38879
hg19879
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045609
Samples
Known GenesEIF3M
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5512148
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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