A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643666



Internal ID21591971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123936097..123936097hg38UCSC Ensembl
chr10:125695613..125695613hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17067613
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643666
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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