A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17007794



Internal ID72825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154280529..154330699hg38UCSC Ensembl
chr7:153977614..154027784hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3850171
hg1950171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492418
Supporting Variants
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17007794
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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