A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4006288



Internal ID22067919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:14072566..14074023hg38UCSC Ensembl
Outerchr9:14067642..14075096hg38UCSC Ensembl
Innerchr9:14072565..14074022hg19UCSC Ensembl
Outerchr9:14067641..14075095hg19UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg387455
hg197455
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154453
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4006288
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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