A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3944159



Internal ID21364228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77316703..77316703hg38UCSC Ensembl
chr13:77890838..77890838hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15194758
SamplesHG002
Known GenesMYCBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3944159
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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