A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5882947



Internal ID22657924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15913468..15917354hg38UCSC Ensembl
chr21:17285788..17289674hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg383887
hg193887
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17487980
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5882947
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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