A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105256



Internal ID22014489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:5043815..5043815hg38UCSC Ensembl
chr21:45639731..45639731hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645607
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105256
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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