A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021107



Internal ID22082738
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 Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156661
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021107
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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