A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17574361



Internal ID21766404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:120078331..120268795hg38UCSC Ensembl
chr7:119718385..119908849hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38190465
hg19190465
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6016125
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17574361
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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