A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17559006



Internal ID21883361
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138650777..138650777hg38UCSC Ensembl
chr7:138335522..138335522hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381245
hg191245
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6067739
Supporting Variants
Samples
Known GenesSVOPL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17559006
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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