A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17094522



Internal ID21410416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:66864649..66864649hg38UCSC Ensembl
chr15:67156987..67156987hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647844
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17094522
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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