A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499072



Internal ID276052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:127405097..127410094hg38UCSC Ensembl
chr11:127274992..127279989hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg384998
hg194998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17051566
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499072
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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