A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4007755



Internal ID22069386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:111262615..111269289hg38UCSC Ensembl
Outerchr9:111260828..111274739hg38UCSC Ensembl
Innerchr9:114024895..114031569hg19UCSC Ensembl
Outerchr9:114023108..114037019hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg3813912
hg1913912
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154532
Supporting Variants
Samples
Known GenesMIR7702
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4007755
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer