A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5597321



Internal ID21545933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89746274..89746362hg38UCSC Ensembl
chr15:90289505..90289593hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17089903
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5597321
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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