A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097436



Internal ID21464594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:95232639..95232639hg38UCSC Ensembl
chr15:95775868..95775868hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5655612
Supporting Variants
SamplesHG03065
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097436
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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