A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2996702



Internal ID16942968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:38849480..38858279hg38UCSC Ensembl
Outerchr4:38851101..38859900hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv950576
Supporting Variants
SamplesBILGI_BIOE
Known GenesTLR6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2996702
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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