A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5628454



Internal ID21576759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:168228148..168228148hg38UCSC Ensembl
chr5:167655153..167655153hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17137448
SamplesHG00732
Known GenesTENM2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5628454
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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