A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877821



Internal ID22652786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:33402908..33409987hg38UCSC Ensembl
chr21:34775214..34782293hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg387080
hg197080
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480310
Samples
Known GenesIFNGR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5877821
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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