A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156633



Internal ID22087034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5473158..5631516hg38UCSC Ensembl
Outerchr7:5471185..5634387hg38UCSC Ensembl
Innerchr7:5512789..5671147hg19UCSC Ensembl
Outerchr7:5510816..5674018hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38163203
hg19163203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4023032
Samples
Known GenesACTB, FBXL18, FSCN1, MIR589, RNF216
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156633
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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