A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5538923



Internal ID313942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35403936..35403936hg38UCSC Ensembl
chr11:35425483..35425483hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044228
Samples
Known GenesSLC1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5538923
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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