A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851332



Internal ID22626267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39087594..39089219hg38UCSC Ensembl
chr11:39109144..39110769hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg381626
hg191626
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17460809
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851332
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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