A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497389



Internal ID274425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40399898..40590224hg38UCSC Ensembl
chr11:40421448..40611774hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38190327
hg19190327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045700
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497389
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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