A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5558679



Internal ID331736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146210814..146215892hg38UCSC Ensembl
chr5:145590377..145595455hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg385079
hg195079
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16974646
Samples
Known GenesRBM27
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5558679
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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