A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14097811



Internal ID21280348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:38349223..38355248hg38UCSC Ensembl
Innerchr17:36505106..36511131hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg386026
hg196026
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3116564
Supporting Variants
Samplessample296
Known GenesSOCS7
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14097811
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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