A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14086781



Internal ID21283729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:106110181..106113371hg38UCSC Ensembl
Innerchr7:105750627..105753817hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg383191
hg193191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3110846
Supporting Variants
Samplessample349
Known GenesSYPL1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14086781
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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