A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5560388



Internal ID333395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:32201749..32203441hg38UCSC Ensembl
chr14:32670955..32672647hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg381693
hg191693
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5560388
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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