A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17098340



Internal ID21500217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40683415..40683541hg38UCSC Ensembl
chr15:40975613..40975739hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603829
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17098340
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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