A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055446



Internal ID21964679
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69065560..69065560hg38UCSC Ensembl
chr2:69292692..69292692hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520676
Samples
Known GenesANTXR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055446
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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