A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857682



Internal ID22632617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73826914..73830938hg38UCSC Ensembl
chr11:73537959..73541983hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg384025
hg194025
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465343
Samples
Known GenesMRPL48
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857682
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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