A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5510153



Internal ID286781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41438685..41438743hg38UCSC Ensembl
chr11:41460235..41460293hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043881
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5510153
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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