A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569459



Internal ID21761502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107253526..107253526hg38UCSC Ensembl
chr7:106893971..106893971hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6080228
Supporting Variants
Samples
Known GenesCOG5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569459
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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