A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3689n100



Internal ID22789776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12772..60213hg38UCSC Ensembl
chr2:12772..60213hg19UCSC Ensembl
chr2:2772..50213hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3847442
hg1947442
hg1847442
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999648, nsv998508, nsv1004654
Samples
Known GenesFAM110C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3689n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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