A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5556887



Internal ID330012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102555781..102576657hg38UCSC Ensembl
chr14:103022118..103042994hg19UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3820877
hg1920877
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17698369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5556887
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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