A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5874221



Internal ID22649172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:26145483..26150131hg38UCSC Ensembl
chr21:27517801..27522449hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg384649
hg194649
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480268
Samples
Known GenesAPP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5874221
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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