A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499659



Internal ID276623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:124929697..124930026hg38UCSC Ensembl
chr11:124799593..124799922hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg38330
hg19330
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17053402
Samples
Known GenesHEPACAM
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499659
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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