A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507736



Internal ID284449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62856771..62875787hg38UCSC Ensembl
chr11:62624243..62643259hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3819017
hg1919017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047884
Samples
Known GenesSLC3A2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507736
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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