A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569314



Internal ID21761357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154058234..154061699hg38UCSC Ensembl
chr7:153755319..153758784hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg383466
hg193466
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000581
Supporting Variants
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569314
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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