A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5559304



Internal ID332341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:27261934..27473136hg38UCSC Ensembl
chr4:27263556..27474758hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg38211203
hg19211203
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16946685
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5559304
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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