A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5855753



Internal ID22630688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:131300705..131305865hg38UCSC Ensembl
chr10:133098968..133104128hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg385161
hg195161
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464474
Samples
Known GenesTCERG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5855753
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