A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005292



Internal ID22066923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:35496317..35546738hg38UCSC Ensembl
Outerchr9:35493487..35551636hg38UCSC Ensembl
Innerchr9:35496314..35546735hg19UCSC Ensembl
Outerchr9:35493484..35551633hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3858150
hg1958150
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154480
Supporting Variants
Samples
Known GenesRUSC2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005292
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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