A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5420331



Internal ID199434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:66141191..66159145hg38UCSC Ensembl
chr9:42362179..42380077hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3817955
hg1917899
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17024132
Samples
Known GenesANKRD20A2, ANKRD20A3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5420331
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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