A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5562503



Internal ID335456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:187891915..188336394hg38UCSC Ensembl
chr4:188813069..189257548hg19UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38444480
hg19444480
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962360
Samples
Known GenesTRIML1, TRIML2, ZFP42
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5562503
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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