A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6060039



Internal ID21969272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:121824695..121824695hg38UCSC Ensembl
chr1:121365329..121365329hg19UCSC Ensembl
Cytoband1p11.2
Allele length
AssemblyAllele length
hg38267
hg19267
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17527796
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6060039
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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