A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5591128



Internal ID21539701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72279586..72283235hg38UCSC Ensembl
chr15:72571927..72575576hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383650
hg193650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17082918
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5591128
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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