A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5561109



Internal ID334096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:58869604..59552865hg38UCSC Ensembl
chr15:59161803..59845064hg19UCSC Ensembl
Cytoband15q22.1
Allele length
AssemblyAllele length
hg38683262
hg19683262
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17700925
Samples
Known GenesCCNB2, FAM81A, LDHAL6B, MIR2116, MYO1E, RNF111, SLTM
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5561109
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer