A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511663



Internal ID288235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:63460657..63460768hg38UCSC Ensembl
chr11:63228129..63228240hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047956
Samples
Known GenesMIR3680-1, MIR3680-2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511663
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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