A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5868282



Internal ID22643217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36053992..36059223hg38UCSC Ensembl
chr21:37426290..37431521hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg385232
hg195232
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488514, nssv17480333
Samples
Known GenesSETD4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5868282
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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