A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090075



Internal ID21491667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51697177..51697289hg38UCSC Ensembl
chr15:51989374..51989486hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38113
hg19113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591301
Supporting Variants
SamplesNA19238
Known GenesSCG3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090075
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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