A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4087n100



Internal ID22790174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:146083669..146109354hg38UCSC Ensembl
chr2:146841237..146866922hg19UCSC Ensembl
chr2:146557707..146583392hg18UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3825686
hg1925686
hg1825686
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007357, nsv1000466
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4087n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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