A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3701n100



Internal ID22789788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1416577..1538526hg38UCSC Ensembl
chr2:1420349..1542298hg19UCSC Ensembl
chr2:1399356..1521305hg18UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38121950
hg19121950
hg18121950
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1007276, nsv997857, nsv1012317, nsv1011997, nsv998563, nsv1007986, nsv1000529
Samples
Known GenesTPO
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3701n100
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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