A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5620793



Internal ID21569098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:64239074..64239074hg38UCSC Ensembl
chr1:64704757..64704757hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38357
hg19357
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17066199
SamplesNA18939
Known GenesUBE2U
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5620793
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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