A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974079



Internal ID22749014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:41411142..41411142hg38UCSC Ensembl
chr11:41432692..41432692hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17365542
Samples
Known GenesLRRC4C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974079
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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