A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879801



Internal ID22654771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:24178820..24202152hg38UCSC Ensembl
chr21:25551133..25574465hg19UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg3823333
hg1923333
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488442
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879801
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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