A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513077



Internal ID289609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63106937..63127977hg38UCSC Ensembl
chr11:62874409..62895449hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3821041
hg1921041
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047907
Samples
Known GenesSLC22A24
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513077
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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