A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3940858



Internal ID21360927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36794664..36794664hg38UCSC Ensembl
chr13:37368801..37368801hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194112
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3940858
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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