A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3711n100



Internal ID22789798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:6103342..6806185hg38UCSC Ensembl
chr2:6243474..6946316hg19UCSC Ensembl
chr2:6160925..6863767hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38702844
hg19702843
hg18702843
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013649, nsv1008599
Samples
Known GenesLINC00487, MIR7515
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3711n100
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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