A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079367



Internal ID21988600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:110947725..110947725hg38UCSC Ensembl
chr5:110283424..110283424hg19UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg38319
hg19319
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544263
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079367
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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