A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560618



Internal ID21884973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116566222..116566222hg38UCSC Ensembl
chr6:116887385..116887385hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080430
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560618
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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