A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061896



Internal ID21971129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63727737..63727737hg38UCSC Ensembl
chr6:64437630..64437630hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560614
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061896
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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