A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5857534



Internal ID22632469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62857706..62859650hg38UCSC Ensembl
chr11:62625178..62627122hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg381945
hg191945
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17459300
Samples
Known GenesSLC3A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5857534
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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