A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5555400



Internal ID328556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79368937..79370232hg38UCSC Ensembl
chr15:79661279..79662574hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg381296
hg191296
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704384
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5555400
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