A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156717



Internal ID22087118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:115943399..115946380hg38UCSC Ensembl
Outerchr7:115942028..115947168hg38UCSC Ensembl
Innerchr7:115583453..115586434hg19UCSC Ensembl
Outerchr7:115582082..115587222hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg385141
hg195141
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022223
Samples
Known GenesTFEC
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156717
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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