A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108395



Internal ID22017629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:38201739..38201739hg38UCSC Ensembl
chr21:39573833..39573833hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17647695
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108395
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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