A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5870620



Internal ID22645556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:39057736..39071268hg38UCSC Ensembl
chr21:40429662..40443194hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3813533
hg1913533
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17488879
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5870620
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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