A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5848279



Internal ID22623214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82732359..82733831hg38UCSC Ensembl
chr11:82443401..82444873hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381473
hg191473
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465144, nssv17462633
Samples
Known GenesFAM181B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5848279
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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