A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562584



Internal ID335533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127112874..127112925hg38UCSC Ensembl
chr11:126982769..126982820hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV line1 insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17051541
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562584
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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