A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867541



Internal ID22642476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:57560009..57561008hg38UCSC Ensembl
chr11:57327482..57328481hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464515
Samples
Known GenesUBE2L6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867541
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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