A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3943877



Internal ID21363946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:39031690..39031690hg38UCSC Ensembl
chr19:39522330..39522330hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15185174
SamplesHG002
Known GenesFBXO27
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3943877
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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