A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5671747



Internal ID21620054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:24341057..24341057hg38UCSC Ensembl
chr21:25713370..25713370hg19UCSC Ensembl
Cytoband21q21.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17118803
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5671747
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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