A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092786



Internal ID21458167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26968283..26968608hg38UCSC Ensembl
chr15:27213430..27213755hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588658
Supporting Variants
SamplesHG02587
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092786
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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