A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103000



Internal ID22012233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32757122..32757122hg38UCSC Ensembl
chr21:34129433..34129433hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17648533
Samples
Known GenesPAXBP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103000
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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