A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4744922



Internal ID20520926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60349820..60350355hg38UCSC Ensembl
chr15:60642019..60642554hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16264171
Samples
Known GenesANXA2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4744922
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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