A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5553959



Internal ID327157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64774850..64783921hg38UCSC Ensembl
chr15:65067049..65076120hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg389072
hg199072
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704231
Samples
Known GenesRBPMS2
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5553959
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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