A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5499954



Internal ID276906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:40014852..40020299hg38UCSC Ensembl
chr11:40036402..40041849hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg385448
hg195448
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045682
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5499954
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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