A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5428224



Internal ID207102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:8987000..8993000hg38UCSC Ensembl
chr21:9825833..9831833hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg386001
hg196001
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17733847
Samples
Known GenesMIR3648, MIR3687
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5428224
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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