A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5623026



Internal ID21571331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28055471..28055471hg38UCSC Ensembl
chr1:28381982..28381982hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17065084
SamplesHG03486
Known GenesEYA3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5623026
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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