A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068599



Internal ID21977832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:137810208..137810208hg38UCSC Ensembl
chr6:138131345..138131345hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381136
hg191136
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568504
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068599
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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