A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560614



Internal ID21884969
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 StatusS
Merged Variantsnsv6061896
Supporting Variants
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560614
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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