A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5504549



Internal ID281349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28360000..28373000hg38UCSC Ensembl
chr11:28381547..28394547hg19UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3813001
hg1913001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044517
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5504549
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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