A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108213



Internal ID22017446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:18815295..18815295hg38UCSC Ensembl
chr21:20187613..20187613hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638931
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108213
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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