A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156661



Internal ID22087062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:47245685..47249326hg38UCSC Ensembl
Outerchr7:47243291..47252356hg38UCSC Ensembl
Innerchr7:47285283..47288924hg19UCSC Ensembl
Outerchr7:47282889..47291954hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg389066
hg199066
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4021107
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156661
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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