A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6078119



Internal ID21987352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:163291160..163291160hg38UCSC Ensembl
chr6:163712192..163712192hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565003
Samples
Known GenesPACRG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6078119
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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