A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082449



Internal ID21490472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68859553..68859856hg38UCSC Ensembl
chr15:69151892..69152195hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595255
Supporting Variants
SamplesNA19238
Known GenesMIR548H4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082449
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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