A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154487



Internal ID22084992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:42726309..42736668hg38UCSC Ensembl
Innerchr9:44241817..44243433hg19UCSC Ensembl
Outerchr9:44234451..44244880hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3810360
hg1910430
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005377, nssv4005380, nssv4005378
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154487
Frequency
Sample Size131
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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