A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5875975



Internal ID22650935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42999421..43000520hg38UCSC Ensembl
chr21:44419531..44420630hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480904
Samples
Known GenesPKNOX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5875975
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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