A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5880602



Internal ID22655572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:32300267..32305547hg38UCSC Ensembl
chr21:33672578..33677858hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg385281
hg195281
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17480301
Samples
Known GenesMRAP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5880602
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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