A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915688



Internal ID22690906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131049156..131126884hg38UCSC Ensembl
chr10:132847419..132925147hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3877729
hg1977729
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17367167
Samples
Known GenesTCERG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915688
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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