A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5603828



Internal ID21552494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:322908..323201hg38UCSC Ensembl
chr10:368848..369141hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38294
hg19294
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17070128
SamplesHG00513
Known GenesDIP2C
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5603828
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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