A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156724



Internal ID22087125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:133202821..133217043hg38UCSC Ensembl
Outerchr7:133199967..133222972hg38UCSC Ensembl
Innerchr7:132887579..132901801hg19UCSC Ensembl
Outerchr7:132884725..132907730hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3823006
hg1923006
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4022326
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1156724
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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