A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862336



Internal ID22637271
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:97965070..97968669hg38UCSC Ensembl
chr11:97835798..97839397hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17468331, nssv17466515
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862336
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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