A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5564078



Internal ID337000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:51361207..51361215hg38UCSC Ensembl
chr14:51827925..51827933hg19UCSC Ensembl
Cytoband14q22.1
Allele length
AssemblyAllele length
hg389
hg199
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17696173
Samples
Known GenesLINC00640
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5564078
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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