A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111789



Internal ID22021023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:38603361..38603361hg38UCSC Ensembl
chr19:39094001..39094001hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17634539
Samples
Known GenesMAP4K1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111789
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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