A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17099271



Internal ID21500051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26417038..26417167hg38UCSC Ensembl
chr15:26662185..26662314hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603989
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17099271
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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