A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3946212



Internal ID21366283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112037178..112037178hg38UCSC Ensembl
chr13:112691492..112691492hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194409
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3946212
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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