A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069223



Internal ID21439732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15178372..15178372hg38UCSC Ensembl
chr10:15220371..15220371hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5641180
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069223
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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