A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5563591



Internal ID336523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173347348..173347420hg38UCSC Ensembl
chr4:174268499..174268571hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16961034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5563591
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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