A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106644



Internal ID22015878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10103050..10103050hg38UCSC Ensembl
chr21:10581078..10581078hg19UCSC Ensembl
Cytoband21p11.2
Allele length
AssemblyAllele length
hg38303
hg19303
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17639495
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106644
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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