A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5641180



Internal ID21589485
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 StatusM
Merged Variants
Supporting Variantsnssv17069223
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5641180
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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