A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853802



Internal ID22628737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:49194220..49200910hg38UCSC Ensembl
chr11:49215772..49222462hg19UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg386691
hg196691
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460487
Samples
Known GenesFOLH1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853802
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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