A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051140



Internal ID21960373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:144488412..144488412hg38UCSC Ensembl
chr2:145245979..145245979hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527208
Samples
Known GenesZEB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051140
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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