A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855146



Internal ID22630081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71260833..71264164hg38UCSC Ensembl
chr11:70971879..70975210hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg383332
hg193332
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17458986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855146
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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