A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3937041



Internal ID21357111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111621615..111621615hg38UCSC Ensembl
chr13:112273962..112273962hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38663
hg19663
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194401
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3937041
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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