A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5512295



Internal ID288853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65756476..65757013hg38UCSC Ensembl
chr11:65523947..65524484hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38538
hg19538
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046776
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5512295
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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