A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6103179



Internal ID22012412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43972805..43972805hg38UCSC Ensembl
chr21:45392686..45392686hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381509
hg191509
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17640018
Samples
Known GenesAGPAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6103179
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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