A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5627044



Internal ID21575349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:1273366..1273366hg38UCSC Ensembl
chr5:1273481..1273481hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38101
hg19101
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17128477
SamplesHG00732
Known GenesTERT
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5627044
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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