A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092430



Internal ID21462865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26842639..26842726hg38UCSC Ensembl
chr15:27087786..27087873hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5592780
Supporting Variants
SamplesHG03009
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092430
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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