A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5508734



Internal ID285418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:25900013..25966326hg38UCSC Ensembl
chr11:25921560..25987873hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3866314
hg1966314
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044409
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5508734
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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