A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103686



Internal ID22012919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38590269..38590269hg38UCSC Ensembl
chr19:39080909..39080909hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382596
hg192596
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17622040
Samples
Known GenesMAP4K1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103686
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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