A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17560619



Internal ID21884974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:66955152..66965465hg38UCSC Ensembl
chr7:66420139..66430452hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3810314
hg1910314
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005898
Supporting Variants
Samples
Known GenesTMEM248
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17560619
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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