A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084529



Internal ID21479255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25898786..25898786hg38UCSC Ensembl
chr15:26143933..26143933hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5659687
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084529
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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