A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5643752



Internal ID21592057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:88214019..88214019hg38UCSC Ensembl
chr10:89973776..89973776hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17071997
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5643752
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