A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095377



Internal ID21479369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:89348567..89348567hg38UCSC Ensembl
chr15:89891798..89891798hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654011
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095377
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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