A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14083934



Internal ID21288134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:1605911..1621416hg38UCSC Ensembl
Innerchr6:1606146..1621651hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3815506
hg1915506
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3114819
Supporting Variants
Samplessample412
Known GenesFOXC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14083934
Frequency
Sample Size467
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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