A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5852380



Internal ID22627315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:92291483..92295119hg38UCSC Ensembl
chr11:92024649..92028285hg19UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg383637
hg193637
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459274
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5852380
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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