A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042059



Internal ID21951384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:240207626..240207626hg38UCSC Ensembl
chr1:240370926..240370926hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520933
Samples
Known GenesFMN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042059
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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