A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506876



Internal ID283611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124613761..124614752hg38UCSC Ensembl
chr11:124483657..124484648hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38992
hg19992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17053706
Samples
Known GenesPANX3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506876
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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