A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847814



Internal ID22622749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:73832140..73838497hg38UCSC Ensembl
chr11:73543185..73549542hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg386358
hg196358
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17456324, nssv17466600
Samples
Known GenesMRPL48
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847814
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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