A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4134n100



Internal ID20155750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:187491962..187680076hg38UCSC Ensembl
chr2:188356689..188544803hg19UCSC Ensembl
chr2:188064934..188253048hg18UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38188115
hg19188115
hg18188115
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014298, nsv1013166, nsv997899
Samples
Known GenesTFPI
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4134n100
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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