A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509340



Internal ID285998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65250021..65257515hg38UCSC Ensembl
chr11:65017492..65024986hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg387495
hg197495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17045190
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509340
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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