A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5932855



Internal ID22708160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64751063..64756243hg38UCSC Ensembl
chr15:65043262..65048442hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385181
hg195181
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17379978
Samples
Known GenesRBPMS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5932855
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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