A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061100



Internal ID21970333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:266890..266890hg38UCSC Ensembl
chr5:267005..267005hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17556439
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061100
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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