A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5589210



Internal ID21537774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25999825..25999898hg38UCSC Ensembl
chr15:26244972..26245045hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17099147
SamplesHG00732
Known GenesLOC100128714
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5589210
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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