A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855311



Internal ID22630246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:49199094..49211994hg38UCSC Ensembl
chr11:49220646..49233546hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg3812901
hg1912901
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459581
Samples
Known GenesFOLH1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855311
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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