A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5878624



Internal ID22653590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40954913..40960785hg38UCSC Ensembl
chr21:42326839..42332711hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg385873
hg195873
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488887
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5878624
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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