A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870266



Internal ID22645202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:34011453..34015052hg38UCSC Ensembl
chr21:35383754..35387353hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg383600
hg193600
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488502
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870266
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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