A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848990



Internal ID22623925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:108106122..108119109hg38UCSC Ensembl
chr11:107976849..107989836hg19UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3812988
hg1912988
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454676
Samples
Known GenesCUL5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848990
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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