A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5879472



Internal ID22654441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43035807..43046044hg38UCSC Ensembl
chr21:44455917..44466154hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3810238
hg1910238
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488911, nssv17488910
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5879472
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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