A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5601293



Internal ID21549938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:86296413..86296475hg38UCSC Ensembl
chr15:86839644..86839706hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17096536
SamplesHG00731
Known GenesAGBL1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5601293
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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