A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6047876



Internal ID21957109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:18925760..18925760hg38UCSC Ensembl
chr1:19252254..19252254hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17534415
Samples
Known GenesIFFO2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6047876
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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