A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559067



Internal ID332112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73853806..73981615hg38UCSC Ensembl
chr4:74719523..74847332hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg38127810
hg19127810
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16952283
Samples
Known GenesCXCL1, PF4, PF4V1
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559067
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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