A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5586010



Internal ID21534559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67838079..67838159hg38UCSC Ensembl
chr15:68130417..68130497hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17097773
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5586010
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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