A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561752



Internal ID334722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:23629192..23629195hg38UCSC Ensembl
chr14:24098401..24098404hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg384
hg194
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17693980
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561752
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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