A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154477



Internal ID22084982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:30620842..30702069hg38UCSC Ensembl
Outerchr9:30620331..30708218hg38UCSC Ensembl
Innerchr9:30620840..30702067hg19UCSC Ensembl
Outerchr9:30620329..30708216hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3887888
hg1987888
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv298n97
Supporting Variantsnssv4005288, nssv4005289
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154477
Frequency
Sample Size131
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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