A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559239



Internal ID332279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120557363..120564719hg38UCSC Ensembl
chr4:121478518..121485874hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg387357
hg197357
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16954495
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559239
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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