A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1057n100



Internal ID20152673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7540419..7639690hg38UCSC Ensembl
chr11:7561650..7660921hg19UCSC Ensembl
chr11:7518226..7617497hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3899272
hg1999272
hg1899272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1039329, nsv1040698
Samples
Known GenesPPFIBP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1057n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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