A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5883191



Internal ID22658169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:44195442..44196817hg38UCSC Ensembl
chr21:45615325..45616700hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg381376
hg191376
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488926
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5883191
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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