A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085535



Internal ID21483351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41172813..41173570hg38UCSC Ensembl
chr15:41465011..41465768hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38758
hg19758
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5604126
Supporting Variants
SamplesHG03732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085535
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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