A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17527208



Internal ID21851565
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 StatusS
Merged Variantsnsv6051140
Supporting Variants
Samples
Known GenesZEB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17527208
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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