A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567097



Internal ID21759140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:49565084..49567835hg38UCSC Ensembl
chr6:49532797..49535548hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg382752
hg192752
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016078
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567097
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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