A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154500



Internal ID22085005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:64510408..64812545hg38UCSC Ensembl
Outerchr9:64510280..64813222hg38UCSC Ensembl
Innerchr9:69522826..69824963hg19UCSC Ensembl
Outerchr9:69522698..69825640hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38302943
hg19302943
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4006506
Samples
Known GenesLOC100133920
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154500
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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