A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086369



Internal ID21410938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64799168..64799247hg38UCSC Ensembl
chr15:65091367..65091446hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5591341
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086369
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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