A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500363



Internal ID277301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119027096..119027626hg38UCSC Ensembl
chr11:118897806..118898336hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg38531
hg19531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17052214
Samples
Known GenesSLC37A4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500363
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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