A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513072



Internal ID289605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61669082..61678498hg38UCSC Ensembl
chr11:61436554..61445970hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg389417
hg199417
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046575
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513072
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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