A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4021104



Internal ID22082735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40057772..40155310hg38UCSC Ensembl
Outerchr7:40050333..40159797hg38UCSC Ensembl
Innerchr7:40097371..40194909hg19UCSC Ensembl
Outerchr7:40089932..40199396hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38109465
hg19109465
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156658
Supporting Variants
Samples
Known GenesC7orf10, CDK13, MPLKIP
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4021104
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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