A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5638374



Internal ID21586679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160635192..160635192hg38UCSC Ensembl
chr5:160062199..160062199hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17131035
SamplesNA12329
Known GenesATP10B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5638374
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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