A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928440



Internal ID21348509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99427145..99427145hg38UCSC Ensembl
chr13:100079399..100079399hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15193038
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928440
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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