A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5631335



Internal ID21579640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91991279..91991279hg38UCSC Ensembl
chr10:93751036..93751036hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17072273
SamplesHG03371
Known GenesBTAF1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5631335
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