A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040698



Internal ID18783229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:7540419..7638062hg38UCSC Ensembl
Innerchr11:7561650..7659293hg19UCSC Ensembl
Innerchr11:7518226..7615869hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3897644
hg1997644
hg1897644
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1057n100
Supporting Variantsnssv3708509
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)nsv1040698
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer