A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6107977



Internal ID22017212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43336435..44419523hg38UCSC Ensembl
chr21:44756315..45839406hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381083089
hg191083092
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17649296
Samples
Known GenesAGPAT3, AIRE, C21orf2, C21orf33, CSTB, DNMT3L, HSF2BP, ICOSLG, LINC00313, LINC00319, LOC284837, MIR6070, PDXK, PFKL, PWP2, RRP1, RRP1B, SIK1, TRAPPC10, TRPM2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6107977
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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