A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5615357



Internal ID21563662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119213660..119213660hg38UCSC Ensembl
chr4:120134815..120134815hg19UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17123425
SamplesHG02818
Known GenesUSP53
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5615357
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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