A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039329



Internal ID18781860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7546374..7639690hg38UCSC Ensembl
Innerchr11:7567605..7660921hg19UCSC Ensembl
Innerchr11:7524181..7617497hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3893317
hg1993317
hg1893317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1057n100
Supporting Variantsnssv3505821
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)nsv1039329
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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