A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5502249



Internal ID279122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60023863..60024568hg38UCSC Ensembl
chr11:59791336..59792041hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg38706
hg19706
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047091
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5502249
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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