A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5557932



Internal ID331010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:53884070..53884072hg38UCSC Ensembl
chr14:54350788..54350790hg19UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg383
hg193
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17694863
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5557932
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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