A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3952781



Internal ID21372850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:35213376..35213376hg38UCSC Ensembl
chr13:35787513..35787513hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194103
SamplesHG002
Known GenesNBEA
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3952781
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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