A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111914



Internal ID22021148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:9801032..9801032hg38UCSC Ensembl
chr4_gl000193_random:68346..68346hg19UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17638948
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111914
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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