A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156738



Internal ID22087139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143223081..143398219hg19UCSC Ensembl
Outerchr7:143218968..143408430hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg19189463
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv270n97
Supporting Variantsnssv4019588
Samples
Known GenesCTAGE15, EPHA1-AS1, FAM115C
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156738
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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