A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847766



Internal ID22622701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62505186..62508285hg38UCSC Ensembl
chr15:62797385..62800484hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471747
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847766
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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