A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511532



Internal ID288109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51053511..51053813hg38UCSC Ensembl
chr14:51520229..51520531hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17695239
Samples
Known GenesTRIM9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511532
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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