A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065108



Internal ID21974341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:114011245..114011245hg38UCSC Ensembl
chr6:114332409..114332409hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576976
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065108
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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