A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852141



Internal ID22627076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18931795..18942331hg38UCSC Ensembl
chr11:18953342..18963878hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3810537
hg1910537
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17455513, nssv17459615, nssv17461497
Samples
Known GenesMRGPRX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852141
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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